{"title":"Albomed","description":"\u003cdiv class=\"snocks-manual-grid\"\u003e\n\n  \u003cdiv class=\"snocks-col\"\u003e\n\n    \u003cdiv class=\"snocks-like-block\"\u003e\n      \u003ch3\u003eBuy Albomed\u003c\/h3\u003e\n      \u003cp\u003eAlbomed is a product line based on sodium hyaluronate for intra-articular use and includes several variants with different concentrations and fill volumes. Anyone who wants to \u003ca href=\"\/en\/collections\/gelenkspritzen\"\u003ebuy Albomed\u003c\/a\u003e should always pay attention to the exact product name. At StakonMed you will find \u003ca href=\"\/en\/products\/albomed-mini-1-x-1-ml\"\u003eAlbomed mini 1 x 1.0 ml\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-standard-1-x-2ml\"\u003eAlbomed Standard 1 x 2.0 ml\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-forte-plus-1-x-2-ml\"\u003eAlbomed Forte Plus 1 x 2.0 ml\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-one-1-x-3-ml\"\u003eAlbomed One 1 x 3.0 ml\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-ultra-one-1-x-4-8-ml\"\u003eAlbomed Ultra One 1 x 4.8 ml\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-standard-50-x-2-ml\"\u003eAlbomed Standard 50 x 2.0 ml\u003c\/a\u003e and \u003ca href=\"\/en\/products\/albomed-innoryos-1-x-2-ml\"\u003eAlbomed Innoryos 1 x 2.0 ml\u003c\/a\u003e.\u003c\/p\u003e\n      \u003cp\u003eEspecially for search queries like “buy Albomed,” “buy Albomed injection,” “Albomed price,” or “Albomed products,” the exact variant is crucial. For medical practices, clinics, and medical care centers in Germany, it is important which fill volume and product version fits the respective need.\u003c\/p\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"snocks-like-block\"\u003e\n      \u003ch3\u003eWhat is Albomed?\u003c\/h3\u003e\n      \u003cp\u003eAlbomed KD Intra-Articular Gel is a product family with highly purified sodium hyaluronate for intra-articular use. The sodium hyaluronate is obtained by bacterial fermentation and is contained in a sterile, isotonic, and pyrogen-free phosphate-buffered saline solution. Depending on the variant, 1 ml contains 10 mg, 16 mg, 22 mg, 25 mg, or 30 mg of sodium hyaluronate.\u003c\/p\u003e\n      \u003cp\u003eThat is why Albomed is often also searched for using terms like “Albomed hyaluron,” “Albomed hyaluronic acid,” or “Albomed prefilled syringe.” However, the decisive factor is always the specific product name, such as \u003ca href=\"\/en\/products\/albomed-standard-1-x-2ml\"\u003eAlbomed Standard\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-forte-plus-1-x-2-ml\"\u003eAlbomed Forte Plus\u003c\/a\u003e, or \u003ca href=\"\/en\/products\/albomed-one-1-x-3-ml\"\u003eAlbomed One\u003c\/a\u003e.\u003c\/p\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"snocks-like-block\"\u003e\n      \u003ch3\u003eHow does Albomed work?\u003c\/h3\u003e\n      \u003cp\u003eA key component of healthy synovial fluid is hyaluronic acid. This natural biopolymer contributes to viscoelasticity and is associated with lubricating and shock-absorbing properties. The sodium hyaluronate contained in \u003ca href=\"\/en\/products\/albomed-mini-1-x-1-ml\"\u003eAlbomed mini\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-standard-1-x-2ml\"\u003eAlbomed Standard\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-forte-plus-1-x-2-ml\"\u003eAlbomed Forte Plus\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-one-1-x-3-ml\"\u003eAlbomed One\u003c\/a\u003e, and \u003ca href=\"\/en\/products\/albomed-ultra-one-1-x-4-8-ml\"\u003eAlbomed Ultra One\u003c\/a\u003e is a salt of hyaluronic acid.\u003c\/p\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"snocks-like-block\"\u003e\n      \u003ch3\u003eWhat is Albomed used for?\u003c\/h3\u003e\n      \u003cp\u003eAccording to the instructions for use, Albomed is intended for pain and mobility restrictions of the joints in degenerative changes of the knee joint and other synovial joints, including osteoarthritis. Thus, the product line is aimed at medical facilities that use intra-articular hyaluronic acid.\u003c\/p\u003e\n      \u003cp\u003eThose searching for “Albomed knee,” “Albomed joint injection,” or “Albomed osteoarthritis” often mean exactly this product group. You can also find other suitable \u003ca href=\"\/en\/collections\/gelenkspritzen\"\u003ejoint injections\u003c\/a\u003e in the range.\u003c\/p\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"snocks-like-block\"\u003e\n      \u003ch3\u003eOverview of Albomed variants\u003c\/h3\u003e\n      \u003cp\u003eThe Albomed range includes several prefilled syringes with different volumes and concentrations. These include \u003ca href=\"\/en\/products\/albomed-mini-1-x-1-ml\"\u003eAlbomed mini 1 x 1.0 ml\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-standard-1-x-2ml\"\u003eAlbomed Standard 1 x 2.0 ml\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-forte-plus-1-x-2-ml\"\u003eAlbomed Forte Plus 1 x 2.0 ml\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-one-1-x-3-ml\"\u003eAlbomed One 1 x 3.0 ml\u003c\/a\u003e, and \u003ca href=\"\/en\/products\/albomed-ultra-one-1-x-4-8-ml\"\u003eAlbomed Ultra One 1 x 4.8 ml\u003c\/a\u003e. For higher practice needs, \u003ca href=\"\/en\/products\/albomed-standard-50-x-2-ml\"\u003eAlbomed Standard 50 x 2.0 ml\u003c\/a\u003e is also available.\u003c\/p\u003e\n    \u003c\/div\u003e\n\n  \u003c\/div\u003e\n\n  \u003cdiv class=\"snocks-col\"\u003e\n\n    \u003cdiv class=\"snocks-like-block\"\u003e\n      \u003ch3\u003eAlbomed at StakonMed\u003c\/h3\u003e\n      \u003cp\u003eSeveral Albomed variants are available in the StakonMed range. The product line covers different fill volumes and package sizes, allowing targeted selection according to practice needs.\u003c\/p\u003e\n      \u003cul\u003e\n        \u003cli\u003e\u003ca href=\"\/en\/products\/albomed-mini-1-x-1-ml\"\u003eAlbomed mini 1 x 1.0 ml\u003c\/a\u003e\u003c\/li\u003e\n        \u003cli\u003e\u003ca href=\"\/en\/products\/albomed-standard-1-x-2ml\"\u003eAlbomed Standard 1 x 2.0 ml\u003c\/a\u003e\u003c\/li\u003e\n        \u003cli\u003e\u003ca href=\"\/en\/products\/albomed-forte-plus-1-x-2-ml\"\u003eAlbomed Forte Plus 1 x 2.0 ml\u003c\/a\u003e\u003c\/li\u003e\n        \u003cli\u003e\u003ca href=\"\/en\/products\/albomed-one-1-x-3-ml\"\u003eAlbomed One 1 x 3.0 ml\u003c\/a\u003e\u003c\/li\u003e\n        \u003cli\u003e\u003ca href=\"\/en\/products\/albomed-ultra-one-1-x-4-8-ml\"\u003eAlbomed Ultra One 1 x 4.8 ml\u003c\/a\u003e\u003c\/li\u003e\n        \u003cli\u003e\u003ca href=\"\/en\/products\/albomed-standard-50-x-2-ml\"\u003eAlbomed Standard 50 x 2.0 ml\u003c\/a\u003e\u003c\/li\u003e\n        \u003cli\u003e\u003ca href=\"\/en\/products\/albomed-innoryos-1-x-2-ml\"\u003eAlbomed Innoryos 1 x 2.0 ml\u003c\/a\u003e\u003c\/li\u003e\n      \u003c\/ul\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"snocks-like-block\"\u003e\n      \u003ch3\u003eAlbomed Standard, Forte Plus, and One\u003c\/h3\u003e\n      \u003cp\u003e\u003ca href=\"\/en\/products\/albomed-standard-1-x-2ml\"\u003eAlbomed Standard 1 x 2.0 ml\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-forte-plus-1-x-2-ml\"\u003eAlbomed Forte Plus 1 x 2.0 ml\u003c\/a\u003e, and \u003ca href=\"\/en\/products\/albomed-one-1-x-3-ml\"\u003eAlbomed One 1 x 3.0 ml\u003c\/a\u003e are among the central variants of the range. Additionally, \u003ca href=\"\/en\/products\/albomed-mini-1-x-1-ml\"\u003eAlbomed mini\u003c\/a\u003e and \u003ca href=\"\/en\/products\/albomed-ultra-one-1-x-4-8-ml\"\u003eAlbomed Ultra One\u003c\/a\u003e offer other fill volumes. Therefore, anyone searching for “Albomed One,” “Albomed Forte Plus,” or “Albomed Standard 2 ml” should always go directly to the appropriate product page.\u003c\/p\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"snocks-like-block\"\u003e\n      \u003ch3\u003eHow often is Albomed used?\u003c\/h3\u003e\n      \u003cp\u003eAccording to the product documents, the hydrogel can be injected intra-articularly 1 to 5 times depending on medical determination. The beneficial effects of a treatment are described in the documents for at least 6 months. Treatment cycles can be repeated if necessary.\u003c\/p\u003e\n      \u003cp\u003eThe respective product documents and application by trained medical professionals are always decisive. Albomed is intended exclusively for use by physicians.\u003c\/p\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"snocks-like-block\"\u003e\n      \u003ch3\u003eWhat to consider when buying Albomed?\u003c\/h3\u003e\n      \u003cp\u003eWhen searching for Albomed, product name, concentration, fill volume, and package size should be checked carefully. It is also relevant whether a single pack like \u003ca href=\"\/en\/products\/albomed-mini-1-x-1-ml\"\u003eAlbomed mini\u003c\/a\u003e, \u003ca href=\"\/en\/products\/albomed-one-1-x-3-ml\"\u003eAlbomed One\u003c\/a\u003e, or \u003ca href=\"\/en\/products\/albomed-ultra-one-1-x-4-8-ml\"\u003eAlbomed Ultra One\u003c\/a\u003e or a larger unit like \u003ca href=\"\/en\/products\/albomed-standard-50-x-2-ml\"\u003eAlbomed Standard 50 x 2.0 ml\u003c\/a\u003e is needed.\u003c\/p\u003e\n      \u003cp\u003eYou can also find more products from the \u003ca href=\"\/en\/collections\/gelenkspritzen\"\u003ejoint injections\u003c\/a\u003e category at StakonMed. For practices and clinics in Germany, a clear standardization of the used variants is advisable to avoid confusion in the ordering process.\u003c\/p\u003e\n    \u003c\/div\u003e\n\n    \u003cdiv class=\"snocks-like-block\"\u003e\n      \u003ch3\u003eFrequently asked questions about Albomed\u003c\/h3\u003e\n      \u003cp\u003e\u003cstrong\u003eWhat is Albomed?\u003c\/strong\u003e\u003cbr\u003eAlbomed is a product line with intra-articularly applicable sodium hyaluronate in the form of prefilled syringes with different concentrations and fill volumes.\u003c\/p\u003e\n      \u003cp\u003e\u003cstrong\u003eWhat is Albomed used for?\u003c\/strong\u003e\u003cbr\u003eAccording to product documents, Albomed is intended for degenerative changes of the knee joint and other synovial joints.\u003c\/p\u003e\n      \u003cp\u003e\u003cstrong\u003eHow often is Albomed used?\u003c\/strong\u003e\u003cbr\u003eDepending on medical determination, Albomed can be injected intra-articularly 1 to 5 times.\u003c\/p\u003e\n      \u003cp\u003e\u003cstrong\u003eWho is allowed to use Albomed?\u003c\/strong\u003e\u003cbr\u003eAlbomed is intended exclusively for use by physicians.\u003c\/p\u003e\n    \u003c\/div\u003e\n\n  \u003c\/div\u003e\n\n\u003c\/div\u003e","products":[{"product_id":"albomed-mini-1-x-1-ml","title":"Albomed mini 1x 1.0 ml","description":"\u003cp\u003e\u003ca href=\"https:\/\/stakonmed.de\/collections\/albomed\" title=\"Albomed | Gelenkspritzen | StakonMed\"\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003c\/a\u003e\u003cspan\u003e\u003ca href=\"https:\/\/stakonmed.de\/collections\/albomed\" title=\"Albomed | Gelenkspritzen | StakonMed\"\u003eGel\u003c\/a\u003e\u003cbr\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eUltra One Gel\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSodium hyaluronate intra-articular\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDescription\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv title=\"Page 1\" class=\"page\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eThe product contains a prefilled syringe with hydrogel made of highly purified sodium hyaluronate obtained by bacterial fermentation without \u003c\/span\u003e\u003cspan\u003esodium hyaluronate obtained from genetic modifications with high molecular weight, which is used to improve \u003c\/span\u003e\u003cspan\u003eserves the viscosity in the intra-articular connective tissue. It has undergone steam sterilization for injectable products and is non-pyrogenic.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv title=\"Page 1\" class=\"page\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eDepending on the product variant and concentration, 1 ml of aqueous, physiological phosphate buffer solution contains 10 mg, \u003c\/span\u003e\u003cspan\u003e16 mg, 22 mg, 25 mg or 30 mg sodium hyaluronate. The sodium hyaluronate hydrogel is in a weak, sterile, isotonic, and apyrogenic phosphate-buffered saline solution with a pH value \u003c\/span\u003e\u003cspan\u003efrom 7.2 (6.8 – 7.4) in sufficient volume for injection. Fill volumes vary depending on the variant from 1 to 4.8 ml. The translation of the chemical components is listed in the table in English (weight per volume as \u003c\/span\u003e\u003cspan\u003emg substance per 1 ml hydrogel):\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv title=\"Page 1\" class=\"page\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e(a) Sodium hyaluronate, (b) Sodium chloride, (c) Disodium hydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO,\u003cbr\u003e(d) Sodium dihydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO, (e) Water for injection purposes\u003cbr\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv title=\"Page 1\" class=\"page\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eProperties and mode of action\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eAn essential component of healthy synovial fluid is the widespread glycosaminoglycan hyaluronic acid. \u003c\/span\u003e\u003cspan\u003eThis natural biopolymer provides viscoelasticity and, thanks to its lubricating and shock-absorbing properties, enables pain-free physiological movements; it also supplies nutrients to the cartilage. The \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003eThe contained sodium hyaluronate is a salt of hyaluronic acid.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv title=\"Page 1\" class=\"page\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eIndications\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv title=\"Page 1\" class=\"page\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePain and limitation of joint mobility in degenerative changes of the knee joint and other synovial joints, including osteoarthritis.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eContraindications\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used in patients\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv title=\"Page 1\" class=\"page\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- with known hypersensitivity to any of the components\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003e- with inflammation in the joint\u003cbr\u003e- with septic arthritis\u003cbr\u003e- with skin infections or skin diseases in the injection area\u003cbr\u003e- with natural or medication-induced coagulation disorders such as hemophilia or under use\u003c\/span\u003e\u003cspan\u003euse of anticoagulants such as Marcumar (phenprocoumon) or Coumadin (warfarin)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv title=\"Page 1\" class=\"page\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eSince there are no clinical data on the use of hyaluronic acid in children, pregnant or breastfeeding women, use in these patients is not recommended.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003ePrecautions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSince septic arthritis can be a serious complication of treatment, please observe all precautions usually necessary for surgical procedures. Injections of the hydrogel must be administered directly into the joint cavity; injections into blood vessels and surrounding tissue must be avoided. Do not use if the prefilled syringe or sterile packaging is damaged.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan style=\"font-size: 0.875rem;\"\u003eThe opened product must not be resterilized, resealed, or reused. It is intended for use by a single patient at a single treatment session.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv title=\"Page 1\" class=\"page\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePossible side effects\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eNo adverse effects were observed in biocompatibility tests with the product. In the treated\u003c\/span\u003e\u003cspan\u003e- affected joint, local symptoms such as pain, redness, warmth, and swelling may occur. \u003c\/span\u003e\u003cspan\u003eThese symptoms can be reduced if the treated area is cooled with an ice pack for 5 to 10 minutes after injection. During the first days of treatment, the simultaneous oral intake of pain and anti-inflammatory medications (NSAIDs) may be beneficial. In cases of intense \u003c\/span\u003e\u003cspan\u003eIf pain or inflammation occurs, treatment should be discontinued. Treatment of adverse reactions should only be carried out under the supervision of the attending physician. Immediately after the injection, strenuous physical activity should be avoided and other instructions from the doctor should be followed. Medical personnel should inform the patient\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv title=\"Page 1\" class=\"page\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- about possible adverse events related to the product.\u003cbr\u003e- that the patient must report any adverse event or complication to a doctor. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003ePharmacological and chemical interactions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSo far, there are no data on the incompatibility of the product with other solutions for intra-articular use.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThere is a chemical incompatibility between sodium hyaluronate and quaternary ammonium compounds. \u003c\/span\u003e\u003cspan\u003esuch as benzalkonium chloride, which can lead to crystalline precipitation. Therefore, this product must never come into contact with surgical instruments or other products that contain these, or with \u003c\/span\u003e\u003cspan\u003eSolutions containing quaternary ammonium compounds as biocidal preservatives. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDosage, type, and duration of use\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe prefilled syringe is to be removed from its packaging. The protective cap is to be removed from the Luer-Lock thread. A suitable sterile injection needle is to be screwed onto the syringe. The use of a single-use needle is recommended. Air should be evacuated from the needle before injection. The skin area intended for injection must be cleaned with an appropriate topical antiseptic. In the case of joint effusion, it is recommended that solutions containing quaternary ammonium compounds as biocidal preservatives be rinsed before injection. \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003einitially reduce the effusion by aspiration and examine it for bacterial etiology. The hydrogel can be injected 1 to 5 times at intervals determined by the physician. \u003c\/span\u003e\u003cspan\u003eInjected intra-articularly at intervals. The beneficial effects of a treatment last at least 6 months. Treatment cycles can be repeated if necessary.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eDepending on the fill volume, several joints of a patient can be treated simultaneously. Unused product must be disposed of.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDosage form\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eA box with one prefilled syringe of 1 ml - 4.8 ml.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDurability\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used after the expiration date. The expiration date (month\/year) is printed on the \u003c\/span\u003e\u003cspan\u003eSyringe blister and printed on the carton.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eStorage instructions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product should be stored dry between 2° and 25°C and protected from light and impact in the original packaging. Accordingly, warning symbols on the packaging must be observed.\u003cbr\u003eKeep the product out of reach of children.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eRecommended user group\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eIntended exclusively for use by physicians.\u003cbr\u003eFor single use only. Do not resterilize. Do not use syringes, needles, or hydrogel from open or damaged packaging or attempt to reseal packaging.\u003cbr\u003eSyringe content is non-toxic and non-flammable.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eWhen using a product from damaged packaging or reusing with other \u003c\/span\u003e\u003cspan\u003epatients or the same patient at a different time are the intended properties and the \u003c\/span\u003e\u003cspan\u003eSterility is not guaranteed. Otherwise, possible transmission of material contamination and pathogens \u003c\/span\u003e\u003cspan\u003efrom the environment, the clinical area, or (other) patients could lead to health complications \u003c\/span\u003e\u003cspan\u003elead to. Resealing or resterilization does not constitute an allowed or guaranteed restoration of \u003c\/span\u003e\u003cspan\u003eusable condition.\u003cbr\u003eUnused syringes and their contents are not infectious and can be disposed of before or after the expiration date, observing national and local regulations. Used syringes and needles must be treated as epidemiologically hazardous waste, and national and local regulations for safe use and disposal must be followed.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv title=\"Page 1\" class=\"page\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eStatus of information 05\/2021\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"ALBOMED GmbH","offers":[{"title":"Default Title","offer_id":47355873689940,"sku":"101","price":25.95,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0786\/8756\/8212\/files\/albomed-mini-albomed-gmbh-gelenkspritzen-stakonmed-795107.jpg?v=1772213474"},{"product_id":"albomed-standard-1-x-2ml","title":"Albomed Standard 1x 2.0 ml","description":"\u003cp\u003e\u003ca title=\"Albomed | Gelenkspritzen | StakonMed\" href=\"https:\/\/stakonmed.de\/collections\/albomed\"\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003c\/a\u003e\u003cspan\u003e\u003ca title=\"Albomed | Gelenkspritzen | StakonMed\" href=\"https:\/\/stakonmed.de\/collections\/albomed\"\u003eGel\u003c\/a\u003e\u003cbr\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eUltra One Gel\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSodium hyaluronate intra-articular\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDescription\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eThe product contains a prefilled syringe with hydrogel made of highly purified sodium hyaluronate obtained by bacterial fermentation without \u003c\/span\u003e\u003cspan\u003esodium hyaluronate obtained from genetic modifications with high molecular weight, which is used to improve \u003c\/span\u003e\u003cspan\u003eserves the viscosity in the intra-articular connective tissue. It has undergone steam sterilization for injectable products and is non-pyrogenic.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eDepending on the product variant and concentration, 1 ml of aqueous, physiological phosphate buffer solution contains 10 mg, \u003c\/span\u003e\u003cspan\u003e16 mg, 22 mg, 25 mg or 30 mg sodium hyaluronate. The sodium hyaluronate hydrogel is in a weak, sterile, isotonic, and apyrogenic phosphate-buffered saline solution with a pH value \u003c\/span\u003e\u003cspan\u003efrom 7.2 (6.8 – 7.4) in sufficient volume for injection. Fill volumes vary depending on the variant from 1 to 4.8 ml. The translation of the chemical components is listed in the table in English (weight per volume as \u003c\/span\u003e\u003cspan\u003emg substance per 1 ml hydrogel):\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e(a) Sodium hyaluronate, (b) Sodium chloride, (c) Disodium hydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO,\u003cbr\u003e(d) Sodium dihydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO, (e) Water for injection purposes\u003cbr\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eProperties and mode of action\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eAn essential component of healthy synovial fluid is the widespread glycosaminoglycan hyaluronic acid. \u003c\/span\u003e\u003cspan\u003eThis natural biopolymer provides viscoelasticity and, thanks to its lubricating and shock-absorbing properties, enables pain-free physiological movements; it also supplies nutrients to the cartilage. The \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003eThe contained sodium hyaluronate is a salt of hyaluronic acid.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eIndications\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePain and limitation of joint mobility in degenerative changes of the knee joint and other synovial joints, including osteoarthritis.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eContraindications\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used in patients\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- with known hypersensitivity to any of the components\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003e- with inflammation in the joint\u003cbr\u003e- with septic arthritis\u003cbr\u003e- with skin infections or skin diseases in the injection area\u003cbr\u003e- with natural or medication-induced coagulation disorders such as hemophilia or under use\u003c\/span\u003e\u003cspan\u003euse of anticoagulants such as Marcumar (phenprocoumon) or Coumadin (warfarin)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eSince there are no clinical data on the use of hyaluronic acid in children, pregnant or breastfeeding women, use in these patients is not recommended.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003ePrecautions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSince septic arthritis can be a serious complication of treatment, please observe all precautions usually necessary for surgical procedures. Injections of the hydrogel must be administered directly into the joint cavity; injections into blood vessels and surrounding tissue must be avoided. Do not use if the prefilled syringe or sterile packaging is damaged.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan style=\"font-size: 0.875rem;\"\u003eThe opened product must not be resterilized, resealed, or reused. It is intended for use by a single patient at a single treatment session.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePossible side effects\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eNo adverse effects were observed in biocompatibility tests with the product. In the treated\u003c\/span\u003e\u003cspan\u003e- affected joint, local symptoms such as pain, redness, warmth, and swelling may occur. \u003c\/span\u003e\u003cspan\u003eThese symptoms can be reduced if the treated area is cooled with an ice pack for 5 to 10 minutes after injection. During the first days of treatment, the simultaneous oral intake of pain and anti-inflammatory medications (NSAIDs) may be beneficial. In cases of intense \u003c\/span\u003e\u003cspan\u003eIf pain or inflammation occurs, treatment should be discontinued. Treatment of adverse reactions should only be carried out under the supervision of the attending physician. Immediately after the injection, strenuous physical activity should be avoided and other instructions from the doctor should be followed. Medical personnel should inform the patient\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- about possible adverse events related to the product.\u003cbr\u003e- that the patient must report any adverse event or complication to a doctor. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003ePharmacological and chemical interactions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSo far, there are no data on the incompatibility of the product with other solutions for intra-articular use.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThere is a chemical incompatibility between sodium hyaluronate and quaternary ammonium compounds. \u003c\/span\u003e\u003cspan\u003esuch as benzalkonium chloride, which can lead to crystalline precipitation. Therefore, this product must never come into contact with surgical instruments or other products that contain these, or with \u003c\/span\u003e\u003cspan\u003eSolutions containing quaternary ammonium compounds as biocidal preservatives. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDosage, type, and duration of use\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe prefilled syringe is to be removed from its packaging. The protective cap is to be removed from the Luer-Lock thread. A suitable sterile injection needle is to be screwed onto the syringe. The use of a single-use needle is recommended. Air should be evacuated from the needle before injection. The skin area intended for injection must be cleaned with an appropriate topical antiseptic. In the case of joint effusion, it is recommended that solutions containing quaternary ammonium compounds as biocidal preservatives be rinsed before injection. \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003einitially reduce the effusion by aspiration and examine it for bacterial etiology. The hydrogel can be injected 1 to 5 times at intervals determined by the physician. \u003c\/span\u003e\u003cspan\u003eInjected intra-articularly at intervals. The beneficial effects of a treatment last at least 6 months. Treatment cycles can be repeated if necessary.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eDepending on the fill volume, several joints of a patient can be treated simultaneously. Unused product must be disposed of.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDosage form\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eA box with one prefilled syringe of 1 ml - 4.8 ml.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDurability\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used after the expiration date. The expiration date (month\/year) is printed on the \u003c\/span\u003e\u003cspan\u003eSyringe blister and printed on the carton.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eStorage instructions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product should be stored dry between 2° and 25°C and protected from light and impact in the original packaging. Accordingly, warning symbols on the packaging must be observed.\u003cbr\u003eKeep the product out of reach of children.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eRecommended user group\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eIntended exclusively for use by physicians.\u003cbr\u003eFor single use only. Do not resterilize. Do not use syringes, needles, or hydrogel from open or damaged packaging or attempt to reseal packaging.\u003cbr\u003eSyringe content is non-toxic and non-flammable.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eWhen using a product from damaged packaging or reusing with other \u003c\/span\u003e\u003cspan\u003epatients or the same patient at a different time are the intended properties and the \u003c\/span\u003e\u003cspan\u003eSterility is not guaranteed. Otherwise, possible transmission of material contamination and pathogens \u003c\/span\u003e\u003cspan\u003efrom the environment, the clinical area, or (other) patients could lead to health complications \u003c\/span\u003e\u003cspan\u003elead to. Resealing or resterilization does not constitute an allowed or guaranteed restoration of \u003c\/span\u003e\u003cspan\u003eusable condition.\u003cbr\u003eUnused syringes and their contents are not infectious and can be disposed of before or after the expiration date, observing national and local regulations. Used syringes and needles must be treated as epidemiologically hazardous waste, and national and local regulations for safe use and disposal must be followed.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eStatus of information 05\/2021\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"ALBOMED GmbH","offers":[{"title":"Default Title","offer_id":47355873722708,"sku":"102","price":29.95,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0786\/8756\/8212\/files\/albomed-standard-albomed-gmbh-gelenkspritzen-stakonmed-488852.jpg?v=1772213626"},{"product_id":"albomed-standard-50-x-2-ml","title":"Albomed Standard 50x 2.0 ml","description":"\u003cp\u003e\u003ca title=\"Albomed | Gelenkspritzen | StakonMed\" href=\"https:\/\/stakonmed.de\/collections\/albomed\"\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003c\/a\u003e\u003cspan\u003e\u003ca title=\"Albomed | Gelenkspritzen | StakonMed\" href=\"https:\/\/stakonmed.de\/collections\/albomed\"\u003eGel\u003c\/a\u003e\u003cbr\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eUltra One Gel\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSodium hyaluronate intra-articular\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDescription\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eThe product contains a prefilled syringe with hydrogel made of highly purified sodium hyaluronate obtained by bacterial fermentation without \u003c\/span\u003e\u003cspan\u003esodium hyaluronate obtained from genetic modifications with high molecular weight, which is used to improve \u003c\/span\u003e\u003cspan\u003eserves the viscosity in the intra-articular connective tissue. It has undergone steam sterilization for injectable products and is non-pyrogenic.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eDepending on the product variant and concentration, 1 ml of aqueous, physiological phosphate buffer solution contains 10 mg, \u003c\/span\u003e\u003cspan\u003e16 mg, 22 mg, 25 mg or 30 mg sodium hyaluronate. The sodium hyaluronate hydrogel is in a weak, sterile, isotonic, and apyrogenic phosphate-buffered saline solution with a pH value \u003c\/span\u003e\u003cspan\u003efrom 7.2 (6.8 – 7.4) in sufficient volume for injection. Fill volumes vary depending on the variant from 1 to 4.8 ml. The translation of the chemical components is listed in the table in English (weight per volume as \u003c\/span\u003e\u003cspan\u003emg substance per 1 ml hydrogel):\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e(a) Sodium hyaluronate, (b) Sodium chloride, (c) Disodium hydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO,\u003cbr\u003e(d) Sodium dihydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO, (e) Water for injection purposes\u003cbr\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eProperties and mode of action\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eAn essential component of healthy synovial fluid is the widespread glycosaminoglycan hyaluronic acid. \u003c\/span\u003e\u003cspan\u003eThis natural biopolymer provides viscoelasticity and, thanks to its lubricating and shock-absorbing properties, enables pain-free physiological movements; it also supplies nutrients to the cartilage. The \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003eThe contained sodium hyaluronate is a salt of hyaluronic acid.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eIndications\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePain and limitation of joint mobility in degenerative changes of the knee joint and other synovial joints, including osteoarthritis.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eContraindications\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used in patients\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- with known hypersensitivity to any of the components\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003e- with inflammation in the joint\u003cbr\u003e- with septic arthritis\u003cbr\u003e- with skin infections or skin diseases in the injection area\u003cbr\u003e- with natural or medication-induced coagulation disorders such as hemophilia or under use\u003c\/span\u003e\u003cspan\u003euse of anticoagulants such as Marcumar (phenprocoumon) or Coumadin (warfarin)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eSince there are no clinical data on the use of hyaluronic acid in children, pregnant or breastfeeding women, use in these patients is not recommended.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003ePrecautions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSince septic arthritis can be a serious complication of treatment, please observe all precautions usually necessary for surgical procedures. Injections of the hydrogel must be administered directly into the joint cavity; injections into blood vessels and surrounding tissue must be avoided. Do not use if the prefilled syringe or sterile packaging is damaged.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan style=\"font-size: 0.875rem;\"\u003eThe opened product must not be resterilized, resealed, or reused. It is intended for use by a single patient at a single treatment session.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePossible side effects\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eNo adverse effects were observed in biocompatibility tests with the product. In the treated\u003c\/span\u003e\u003cspan\u003e- affected joint, local symptoms such as pain, redness, warmth, and swelling may occur. \u003c\/span\u003e\u003cspan\u003eThese symptoms can be reduced if the treated area is cooled with an ice pack for 5 to 10 minutes after injection. During the first days of treatment, the simultaneous oral intake of pain and anti-inflammatory medications (NSAIDs) may be beneficial. In cases of intense \u003c\/span\u003e\u003cspan\u003eIf pain or inflammation occurs, treatment should be discontinued. Treatment of adverse reactions should only be carried out under the supervision of the attending physician. Immediately after the injection, strenuous physical activity should be avoided and other instructions from the doctor should be followed. Medical personnel should inform the patient\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- about possible adverse events related to the product.\u003cbr\u003e- that the patient must report any adverse event or complication to a doctor. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003ePharmacological and chemical interactions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSo far, there are no data on the incompatibility of the product with other solutions for intra-articular use.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThere is a chemical incompatibility between sodium hyaluronate and quaternary ammonium compounds. \u003c\/span\u003e\u003cspan\u003esuch as benzalkonium chloride, which can lead to crystalline precipitation. Therefore, this product must never come into contact with surgical instruments or other products that contain these, or with \u003c\/span\u003e\u003cspan\u003eSolutions containing quaternary ammonium compounds as biocidal preservatives. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDosage, type, and duration of use\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe prefilled syringe is to be removed from its packaging. The protective cap is to be removed from the Luer-Lock thread. A suitable sterile injection needle is to be screwed onto the syringe. The use of a single-use needle is recommended. Air should be evacuated from the needle before injection. The skin area intended for injection must be cleaned with an appropriate topical antiseptic. In the case of joint effusion, it is recommended that solutions containing quaternary ammonium compounds as biocidal preservatives be rinsed before injection. \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003einitially reduce the effusion by aspiration and examine it for bacterial etiology. The hydrogel can be injected 1 to 5 times at intervals determined by the physician. \u003c\/span\u003e\u003cspan\u003eInjected intra-articularly at intervals. The beneficial effects of a treatment last at least 6 months. Treatment cycles can be repeated if necessary.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eDepending on the fill volume, several joints of a patient can be treated simultaneously. Unused product must be disposed of.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDosage form\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eA box with one prefilled syringe of 1 ml - 4.8 ml.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDurability\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used after the expiration date. The expiration date (month\/year) is printed on the \u003c\/span\u003e\u003cspan\u003eSyringe blister and printed on the carton.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eStorage instructions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product should be stored dry between 2° and 25°C and protected from light and impact in the original packaging. Accordingly, warning symbols on the packaging must be observed.\u003cbr\u003eKeep the product out of reach of children.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eRecommended user group\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eIntended exclusively for use by physicians.\u003cbr\u003eFor single use only. Do not resterilize. Do not use syringes, needles, or hydrogel from open or damaged packaging or attempt to reseal packaging.\u003cbr\u003eSyringe content is non-toxic and non-flammable.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eWhen using a product from damaged packaging or reusing with other \u003c\/span\u003e\u003cspan\u003epatients or the same patient at a different time are the intended properties and the \u003c\/span\u003e\u003cspan\u003eSterility is not guaranteed. Otherwise, possible transmission of material contamination and pathogens \u003c\/span\u003e\u003cspan\u003efrom the environment, the clinical area, or (other) patients could lead to health complications \u003c\/span\u003e\u003cspan\u003elead to. Resealing or resterilization does not constitute an allowed or guaranteed restoration of \u003c\/span\u003e\u003cspan\u003eusable condition.\u003cbr\u003eUnused syringes and their contents are not infectious and can be disposed of before or after the expiration date, observing national and local regulations. Used syringes and needles must be treated as epidemiologically hazardous waste, and national and local regulations for safe use and disposal must be followed.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eStatus of information 05\/2021\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"ALBOMED GmbH","offers":[{"title":"Default Title","offer_id":47355873755476,"sku":"103","price":1247.5,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0786\/8756\/8212\/files\/albomed-standard-50x-20-ml-albomed-gmbh-gelenkspritzen-stakonmed-9575618.jpg?v=1772274020"},{"product_id":"albomed-forte-plus-1-x-2-ml","title":"Albomed Forte Plus 1x 2.0 ml","description":"\u003cdiv title=\"Page 1\" class=\"page\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003ca title=\"Albomed | Gelenkspritzen | StakonMed\" href=\"https:\/\/stakonmed.de\/collections\/albomed\"\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003c\/a\u003e\u003cspan\u003e\u003ca title=\"Albomed | Gelenkspritzen | StakonMed\" href=\"https:\/\/stakonmed.de\/collections\/albomed\"\u003eGel\u003c\/a\u003e\u003cbr\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eUltra One Gel\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSodium hyaluronate intra-articular\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDescription\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eThe product contains a prefilled syringe with hydrogel made of highly purified sodium hyaluronate obtained by bacterial fermentation without \u003c\/span\u003e\u003cspan\u003esodium hyaluronate obtained from genetic modifications with high molecular weight, which is used to improve \u003c\/span\u003e\u003cspan\u003eserves the viscosity in the intra-articular connective tissue. It has undergone steam sterilization for injectable products and is non-pyrogenic.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eDepending on the product variant and concentration, 1 ml of aqueous, physiological phosphate buffer solution contains 10 mg, \u003c\/span\u003e\u003cspan\u003e16 mg, 22 mg, 25 mg or 30 mg sodium hyaluronate. The sodium hyaluronate hydrogel is in a weak, sterile, isotonic, and apyrogenic phosphate-buffered saline solution with a pH value \u003c\/span\u003e\u003cspan\u003efrom 7.2 (6.8 – 7.4) in sufficient volume for injection. Fill volumes vary depending on the variant from 1 to 4.8 ml. The translation of the chemical components is listed in the table in English (weight per volume as \u003c\/span\u003e\u003cspan\u003emg substance per 1 ml hydrogel):\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e(a) Sodium hyaluronate, (b) Sodium chloride, (c) Disodium hydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO,\u003cbr\u003e(d) Sodium dihydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO, (e) Water for injection purposes\u003cbr\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eProperties and mode of action\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eAn essential component of healthy synovial fluid is the widespread glycosaminoglycan hyaluronic acid. \u003c\/span\u003e\u003cspan\u003eThis natural biopolymer provides viscoelasticity and, thanks to its lubricating and shock-absorbing properties, enables pain-free physiological movements; it also supplies nutrients to the cartilage. The \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003eThe contained sodium hyaluronate is a salt of hyaluronic acid.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eIndications\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePain and limitation of joint mobility in degenerative changes of the knee joint and other synovial joints, including osteoarthritis.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eContraindications\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used in patients\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- with known hypersensitivity to any of the components\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003e- with inflammation in the joint\u003cbr\u003e- with septic arthritis\u003cbr\u003e- with skin infections or skin diseases in the injection area\u003cbr\u003e- with natural or medication-induced coagulation disorders such as hemophilia or under use\u003c\/span\u003e\u003cspan\u003euse of anticoagulants such as Marcumar (phenprocoumon) or Coumadin (warfarin)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eSince there are no clinical data on the use of hyaluronic acid in children, pregnant or breastfeeding women, use in these patients is not recommended.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003ePrecautions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSince septic arthritis can be a serious complication of treatment, please observe all precautions usually necessary for surgical procedures. Injections of the hydrogel must be administered directly into the joint cavity; injections into blood vessels and surrounding tissue must be avoided. Do not use if the prefilled syringe or sterile packaging is damaged.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan style=\"font-size: 0.875rem;\"\u003eThe opened product must not be resterilized, resealed, or reused. It is intended for use by a single patient at a single treatment session.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePossible side effects\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eNo adverse effects were observed in biocompatibility tests with the product. In the treated\u003c\/span\u003e\u003cspan\u003e- affected joint, local symptoms such as pain, redness, warmth, and swelling may occur. \u003c\/span\u003e\u003cspan\u003eThese symptoms can be reduced if the treated area is cooled with an ice pack for 5 to 10 minutes after injection. During the first days of treatment, the simultaneous oral intake of pain and anti-inflammatory medications (NSAIDs) may be beneficial. In cases of intense \u003c\/span\u003e\u003cspan\u003eIf pain or inflammation occurs, treatment should be discontinued. Treatment of adverse reactions should only be carried out under the supervision of the attending physician. Immediately after the injection, strenuous physical activity should be avoided and other instructions from the doctor should be followed. Medical personnel should inform the patient\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- about possible adverse events related to the product.\u003cbr\u003e- that the patient must report any adverse event or complication to a doctor. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003ePharmacological and chemical interactions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSo far, there are no data on the incompatibility of the product with other solutions for intra-articular use.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThere is a chemical incompatibility between sodium hyaluronate and quaternary ammonium compounds. \u003c\/span\u003e\u003cspan\u003esuch as benzalkonium chloride, which can lead to crystalline precipitation. Therefore, this product must never come into contact with surgical instruments or other products that contain these, or with \u003c\/span\u003e\u003cspan\u003eSolutions containing quaternary ammonium compounds as biocidal preservatives. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDosage, type, and duration of use\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe prefilled syringe is to be removed from its packaging. The protective cap is to be removed from the Luer-Lock thread. A suitable sterile injection needle is to be screwed onto the syringe. The use of a single-use needle is recommended. Air should be evacuated from the needle before injection. The skin area intended for injection must be cleaned with an appropriate topical antiseptic. In the case of joint effusion, it is recommended that solutions containing quaternary ammonium compounds as biocidal preservatives be rinsed before injection. \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003einitially reduce the effusion by aspiration and examine it for bacterial etiology. The hydrogel can be injected 1 to 5 times at intervals determined by the physician. \u003c\/span\u003e\u003cspan\u003eInjected intra-articularly at intervals. The beneficial effects of a treatment last at least 6 months. Treatment cycles can be repeated if necessary.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eDepending on the fill volume, several joints of a patient can be treated simultaneously. Unused product must be disposed of.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDosage form\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eA box with one prefilled syringe of 1 ml - 4.8 ml.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDurability\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used after the expiration date. The expiration date (month\/year) is printed on the \u003c\/span\u003e\u003cspan\u003eSyringe blister and printed on the carton.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eStorage instructions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product should be stored dry between 2° and 25°C and protected from light and impact in the original packaging. Accordingly, warning symbols on the packaging must be observed.\u003cbr\u003eKeep the product out of reach of children.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eRecommended user group\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eIntended exclusively for use by physicians.\u003cbr\u003eFor single use only. Do not resterilize. Do not use syringes, needles, or hydrogel from open or damaged packaging or attempt to reseal packaging.\u003cbr\u003eSyringe content is non-toxic and non-flammable.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eWhen using a product from damaged packaging or reusing with other \u003c\/span\u003e\u003cspan\u003epatients or the same patient at a different time are the intended properties and the \u003c\/span\u003e\u003cspan\u003eSterility is not guaranteed. Otherwise, possible transmission of material contamination and pathogens \u003c\/span\u003e\u003cspan\u003efrom the environment, the clinical area, or (other) patients could lead to health complications \u003c\/span\u003e\u003cspan\u003elead to. Resealing or resterilization does not constitute an allowed or guaranteed restoration of \u003c\/span\u003e\u003cspan\u003eusable condition.\u003cbr\u003eUnused syringes and their contents are not infectious and can be disposed of before or after the expiration date, observing national and local regulations. Used syringes and needles must be treated as epidemiologically hazardous waste, and national and local regulations for safe use and disposal must be followed.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eStatus of information 05\/2021\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"ALBOMED GmbH","offers":[{"title":"Default Title","offer_id":47355879031124,"sku":"104","price":71.95,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0786\/8756\/8212\/files\/albomed-forte-plus-albomed-gmbh-gelenkspritzen-stakonmed-555514.jpg?v=1772213811"},{"product_id":"albomed-one-1-x-3-ml","title":"Albomed One 1x 3.0 ml","description":"\u003cp\u003e\u003ca title=\"Albomed | Gelenkspritzen | StakonMed\" href=\"https:\/\/stakonmed.de\/collections\/albomed\"\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003c\/a\u003e\u003cspan\u003e\u003ca title=\"Albomed | Gelenkspritzen | StakonMed\" href=\"https:\/\/stakonmed.de\/collections\/albomed\"\u003eGel\u003c\/a\u003e\u003cbr\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eUltra One Gel\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSodium hyaluronate intra-articular\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDescription\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eThe product contains a prefilled syringe with hydrogel made of highly purified sodium hyaluronate obtained by bacterial fermentation without \u003c\/span\u003e\u003cspan\u003esodium hyaluronate obtained from genetic modifications with high molecular weight, which is used to improve \u003c\/span\u003e\u003cspan\u003eserves the viscosity in the intra-articular connective tissue. It has undergone steam sterilization for injectable products and is non-pyrogenic.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eDepending on the product variant and concentration, 1 ml of aqueous, physiological phosphate buffer solution contains 10 mg, \u003c\/span\u003e\u003cspan\u003e16 mg, 22 mg, 25 mg or 30 mg sodium hyaluronate. The sodium hyaluronate hydrogel is in a weak, sterile, isotonic, and apyrogenic phosphate-buffered saline solution with a pH value \u003c\/span\u003e\u003cspan\u003efrom 7.2 (6.8 – 7.4) in sufficient volume for injection. Fill volumes vary depending on the variant from 1 to 4.8 ml. The translation of the chemical components is listed in the table in English (weight per volume as \u003c\/span\u003e\u003cspan\u003emg substance per 1 ml hydrogel):\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e(a) Sodium hyaluronate, (b) Sodium chloride, (c) Disodium hydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO,\u003cbr\u003e(d) Sodium dihydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO, (e) Water for injection purposes\u003cbr\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eProperties and mode of action\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eAn essential component of healthy synovial fluid is the widespread glycosaminoglycan hyaluronic acid. \u003c\/span\u003e\u003cspan\u003eThis natural biopolymer provides viscoelasticity and, thanks to its lubricating and shock-absorbing properties, enables pain-free physiological movements; it also supplies nutrients to the cartilage. The \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003eThe contained sodium hyaluronate is a salt of hyaluronic acid.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eIndications\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePain and limitation of joint mobility in degenerative changes of the knee joint and other synovial joints, including osteoarthritis.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eContraindications\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used in patients\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- with known hypersensitivity to any of the components\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003e- with inflammation in the joint\u003cbr\u003e- with septic arthritis\u003cbr\u003e- with skin infections or skin diseases in the injection area\u003cbr\u003e- with natural or medication-induced coagulation disorders such as hemophilia or under use\u003c\/span\u003e\u003cspan\u003euse of anticoagulants such as Marcumar (phenprocoumon) or Coumadin (warfarin)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eSince there are no clinical data on the use of hyaluronic acid in children, pregnant or breastfeeding women, use in these patients is not recommended.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003ePrecautions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSince septic arthritis can be a serious complication of treatment, please observe all precautions usually necessary for surgical procedures. Injections of the hydrogel must be administered directly into the joint cavity; injections into blood vessels and surrounding tissue must be avoided. Do not use if the prefilled syringe or sterile packaging is damaged.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan style=\"font-size: 0.875rem;\"\u003eThe opened product must not be resterilized, resealed, or reused. It is intended for use by a single patient at a single treatment session.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePossible side effects\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eNo adverse effects were observed in biocompatibility tests with the product. In the treated\u003c\/span\u003e\u003cspan\u003e- affected joint, local symptoms such as pain, redness, warmth, and swelling may occur. \u003c\/span\u003e\u003cspan\u003eThese symptoms can be reduced if the treated area is cooled with an ice pack for 5 to 10 minutes after injection. During the first days of treatment, the simultaneous oral intake of pain and anti-inflammatory medications (NSAIDs) may be beneficial. In cases of intense \u003c\/span\u003e\u003cspan\u003eIf pain or inflammation occurs, treatment should be discontinued. Treatment of adverse reactions should only be carried out under the supervision of the attending physician. Immediately after the injection, strenuous physical activity should be avoided and other instructions from the doctor should be followed. Medical personnel should inform the patient\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- about possible adverse events related to the product.\u003cbr\u003e- that the patient must report any adverse event or complication to a doctor. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003ePharmacological and chemical interactions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSo far, there are no data on the incompatibility of the product with other solutions for intra-articular use.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThere is a chemical incompatibility between sodium hyaluronate and quaternary ammonium compounds. \u003c\/span\u003e\u003cspan\u003esuch as benzalkonium chloride, which can lead to crystalline precipitation. Therefore, this product must never come into contact with surgical instruments or other products that contain these, or with \u003c\/span\u003e\u003cspan\u003eSolutions containing quaternary ammonium compounds as biocidal preservatives. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDosage, type, and duration of use\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe prefilled syringe is to be removed from its packaging. The protective cap is to be removed from the Luer-Lock thread. A suitable sterile injection needle is to be screwed onto the syringe. The use of a single-use needle is recommended. Air should be evacuated from the needle before injection. The skin area intended for injection must be cleaned with an appropriate topical antiseptic. In the case of joint effusion, it is recommended that solutions containing quaternary ammonium compounds as biocidal preservatives be rinsed before injection. \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003einitially reduce the effusion by aspiration and examine it for bacterial etiology. The hydrogel can be injected 1 to 5 times at intervals determined by the physician. \u003c\/span\u003e\u003cspan\u003eInjected intra-articularly at intervals. The beneficial effects of a treatment last at least 6 months. Treatment cycles can be repeated if necessary.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eDepending on the fill volume, several joints of a patient can be treated simultaneously. Unused product must be disposed of.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDosage form\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eA box with one prefilled syringe of 1 ml - 4.8 ml.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDurability\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used after the expiration date. The expiration date (month\/year) is printed on the \u003c\/span\u003e\u003cspan\u003eSyringe blister and printed on the carton.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eStorage instructions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product should be stored dry between 2° and 25°C and protected from light and impact in the original packaging. Accordingly, warning symbols on the packaging must be observed.\u003cbr\u003eKeep the product out of reach of children.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eRecommended user group\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eIntended exclusively for use by physicians.\u003cbr\u003eFor single use only. Do not resterilize. Do not use syringes, needles, or hydrogel from open or damaged packaging or attempt to reseal packaging.\u003cbr\u003eSyringe content is non-toxic and non-flammable.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eWhen using a product from damaged packaging or reusing with other \u003c\/span\u003e\u003cspan\u003epatients or the same patient at a different time are the intended properties and the \u003c\/span\u003e\u003cspan\u003eSterility is not guaranteed. Otherwise, possible transmission of material contamination and pathogens \u003c\/span\u003e\u003cspan\u003efrom the environment, the clinical area, or (other) patients could lead to health complications \u003c\/span\u003e\u003cspan\u003elead to. Resealing or resterilization does not constitute an allowed or guaranteed restoration of \u003c\/span\u003e\u003cspan\u003eusable condition.\u003cbr\u003eUnused syringes and their contents are not infectious and can be disposed of before or after the expiration date, observing national and local regulations. Used syringes and needles must be treated as epidemiologically hazardous waste, and national and local regulations for safe use and disposal must be followed.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eStatus of information 05\/2021\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"ALBOMED GmbH","offers":[{"title":"Default Title","offer_id":47355879063892,"sku":"105","price":134.95,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0786\/8756\/8212\/files\/albomed-one-albomed-gmbh-gelenkspritzen-stakonmed-351413.jpg?v=1772213495"},{"product_id":"albomed-ultra-one-1-x-4-8-ml","title":"Albomed Ultra One 1x 4.8 ml","description":"\u003cp\u003e\u003ca title=\"Albomed | Gelenkspritzen | StakonMed\" href=\"https:\/\/stakonmed.de\/collections\/albomed\"\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003c\/a\u003e\u003cspan\u003e\u003ca title=\"Albomed | Gelenkspritzen | StakonMed\" href=\"https:\/\/stakonmed.de\/collections\/albomed\"\u003eGel\u003c\/a\u003e\u003cbr\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eUltra One Gel\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSodium hyaluronate intra-articular\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDescription\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eThe product contains a prefilled syringe with hydrogel made of highly purified sodium hyaluronate obtained by bacterial fermentation without \u003c\/span\u003e\u003cspan\u003esodium hyaluronate obtained from genetic modifications with high molecular weight, which is used to improve \u003c\/span\u003e\u003cspan\u003eserves the viscosity in the intra-articular connective tissue. It has undergone steam sterilization for injectable products and is non-pyrogenic.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eDepending on the product variant and concentration, 1 ml of aqueous, physiological phosphate buffer solution contains 10 mg, \u003c\/span\u003e\u003cspan\u003e16 mg, 22 mg, 25 mg or 30 mg sodium hyaluronate. The sodium hyaluronate hydrogel is in a weak, sterile, isotonic, and apyrogenic phosphate-buffered saline solution with a pH value \u003c\/span\u003e\u003cspan\u003efrom 7.2 (6.8 – 7.4) in sufficient volume for injection. Fill volumes vary depending on the variant from 1 to 4.8 ml. The translation of the chemical components is listed in the table in English (weight per volume as \u003c\/span\u003e\u003cspan\u003emg substance per 1 ml hydrogel):\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e(a) Sodium hyaluronate, (b) Sodium chloride, (c) Disodium hydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO,\u003cbr\u003e(d) Sodium dihydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO, (e) Water for injection purposes\u003cbr\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eProperties and mode of action\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eAn essential component of healthy synovial fluid is the widespread glycosaminoglycan hyaluronic acid. \u003c\/span\u003e\u003cspan\u003eThis natural biopolymer provides viscoelasticity and, thanks to its lubricating and shock-absorbing properties, enables pain-free physiological movements; it also supplies nutrients to the cartilage. The \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003eThe contained sodium hyaluronate is a salt of hyaluronic acid.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eIndications\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePain and limitation of joint mobility in degenerative changes of the knee joint and other synovial joints, including osteoarthritis.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eContraindications\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used in patients\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- with known hypersensitivity to any of the components\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003e- with inflammation in the joint\u003cbr\u003e- with septic arthritis\u003cbr\u003e- with skin infections or skin diseases in the injection area\u003cbr\u003e- with natural or medication-induced coagulation disorders such as hemophilia or under use\u003c\/span\u003e\u003cspan\u003euse of anticoagulants such as Marcumar (phenprocoumon) or Coumadin (warfarin)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eSince there are no clinical data on the use of hyaluronic acid in children, pregnant or breastfeeding women, use in these patients is not recommended.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003ePrecautions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSince septic arthritis can be a serious complication of treatment, please observe all precautions usually necessary for surgical procedures. Injections of the hydrogel must be administered directly into the joint cavity; injections into blood vessels and surrounding tissue must be avoided. Do not use if the prefilled syringe or sterile packaging is damaged.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan style=\"font-size: 0.875rem;\"\u003eThe opened product must not be resterilized, resealed, or reused. It is intended for use by a single patient at a single treatment session.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePossible side effects\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eNo adverse effects were observed in biocompatibility tests with the product. In the treated\u003c\/span\u003e\u003cspan\u003e- affected joint, local symptoms such as pain, redness, warmth, and swelling may occur. \u003c\/span\u003e\u003cspan\u003eThese symptoms can be reduced if the treated area is cooled with an ice pack for 5 to 10 minutes after injection. During the first days of treatment, the simultaneous oral intake of pain and anti-inflammatory medications (NSAIDs) may be beneficial. In cases of intense \u003c\/span\u003e\u003cspan\u003eIf pain or inflammation occurs, treatment should be discontinued. Treatment of adverse reactions should only be carried out under the supervision of the attending physician. Immediately after the injection, strenuous physical activity should be avoided and other instructions from the doctor should be followed. Medical personnel should inform the patient\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- about possible adverse events related to the product.\u003cbr\u003e- that the patient must report any adverse event or complication to a doctor. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003ePharmacological and chemical interactions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSo far, there are no data on the incompatibility of the product with other solutions for intra-articular use.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThere is a chemical incompatibility between sodium hyaluronate and quaternary ammonium compounds. \u003c\/span\u003e\u003cspan\u003esuch as benzalkonium chloride, which can lead to crystalline precipitation. Therefore, this product must never come into contact with surgical instruments or other products that contain these, or with \u003c\/span\u003e\u003cspan\u003eSolutions containing quaternary ammonium compounds as biocidal preservatives. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDosage, type, and duration of use\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe prefilled syringe is to be removed from its packaging. The protective cap is to be removed from the Luer-Lock thread. A suitable sterile injection needle is to be screwed onto the syringe. The use of a single-use needle is recommended. Air should be evacuated from the needle before injection. The skin area intended for injection must be cleaned with an appropriate topical antiseptic. In the case of joint effusion, it is recommended that solutions containing quaternary ammonium compounds as biocidal preservatives be rinsed before injection. \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003einitially reduce the effusion by aspiration and examine it for bacterial etiology. The hydrogel can be injected 1 to 5 times at intervals determined by the physician. \u003c\/span\u003e\u003cspan\u003eInjected intra-articularly at intervals. The beneficial effects of a treatment last at least 6 months. Treatment cycles can be repeated if necessary.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eDepending on the fill volume, several joints of a patient can be treated simultaneously. Unused product must be disposed of.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDosage form\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eA box with one prefilled syringe of 1 ml - 4.8 ml.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDurability\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used after the expiration date. The expiration date (month\/year) is printed on the \u003c\/span\u003e\u003cspan\u003eSyringe blister and printed on the carton.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eStorage instructions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product should be stored dry between 2° and 25°C and protected from light and impact in the original packaging. Accordingly, warning symbols on the packaging must be observed.\u003cbr\u003eKeep the product out of reach of children.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eRecommended user group\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eIntended exclusively for use by physicians.\u003cbr\u003eFor single use only. Do not resterilize. Do not use syringes, needles, or hydrogel from open or damaged packaging or attempt to reseal packaging.\u003cbr\u003eSyringe content is non-toxic and non-flammable.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eWhen using a product from damaged packaging or reusing with other \u003c\/span\u003e\u003cspan\u003epatients or the same patient at a different time are the intended properties and the \u003c\/span\u003e\u003cspan\u003eSterility is not guaranteed. Otherwise, possible transmission of material contamination and pathogens \u003c\/span\u003e\u003cspan\u003efrom the environment, the clinical area, or (other) patients could lead to health complications \u003c\/span\u003e\u003cspan\u003elead to. Resealing or resterilization does not constitute an allowed or guaranteed restoration of \u003c\/span\u003e\u003cspan\u003eusable condition.\u003cbr\u003eUnused syringes and their contents are not infectious and can be disposed of before or after the expiration date, observing national and local regulations. Used syringes and needles must be treated as epidemiologically hazardous waste, and national and local regulations for safe use and disposal must be followed.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eStatus of information 05\/2021\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"ALBOMED GmbH","offers":[{"title":"Default Title","offer_id":47355879326036,"sku":"106","price":149.95,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0786\/8756\/8212\/files\/albomed-ultra-one-albomed-gmbh-gelenkspritzen-stakonmed-374730.jpg?v=1772213914"},{"product_id":"albomed-innoryos-1-x-2-ml","title":"Albomed Innoryos 1x 2.0 ml","description":"\u003cp\u003e\u003ca title=\"Albomed | Gelenkspritzen | StakonMed\" href=\"https:\/\/stakonmed.de\/collections\/albomed\"\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003c\/a\u003e\u003cspan\u003e\u003ca title=\"Albomed | Gelenkspritzen | StakonMed\" href=\"https:\/\/stakonmed.de\/collections\/albomed\"\u003eGel\u003c\/a\u003e\u003cbr\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eUltra One Gel\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSodium hyaluronate intra-articular\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDescription\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eThe product contains a prefilled syringe with hydrogel made of highly purified sodium hyaluronate obtained by bacterial fermentation without \u003c\/span\u003e\u003cspan\u003esodium hyaluronate obtained from genetic modifications with high molecular weight, which is used to improve \u003c\/span\u003e\u003cspan\u003eserves the viscosity in the intra-articular connective tissue. It has undergone steam sterilization for injectable products and is non-pyrogenic.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eDepending on the product variant and concentration, 1 ml of aqueous, physiological phosphate buffer solution contains 10 mg, \u003c\/span\u003e\u003cspan\u003e16 mg, 22 mg, 25 mg or 30 mg sodium hyaluronate. The sodium hyaluronate hydrogel is in a weak, sterile, isotonic, and apyrogenic phosphate-buffered saline solution with a pH value \u003c\/span\u003e\u003cspan\u003efrom 7.2 (6.8 – 7.4) in sufficient volume for injection. Fill volumes vary depending on the variant from 1 to 4.8 ml. The translation of the chemical components is listed in the table in English (weight per volume as \u003c\/span\u003e\u003cspan\u003emg substance per 1 ml hydrogel):\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e(a) Sodium hyaluronate, (b) Sodium chloride, (c) Disodium hydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO,\u003cbr\u003e(d) Sodium dihydrogen phosphate 2 H\u003c\/span\u003e\u003cspan\u003e2\u003c\/span\u003e\u003cspan\u003eO, (e) Water for injection purposes\u003cbr\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eProperties and mode of action\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eAn essential component of healthy synovial fluid is the widespread glycosaminoglycan hyaluronic acid. \u003c\/span\u003e\u003cspan\u003eThis natural biopolymer provides viscoelasticity and, thanks to its lubricating and shock-absorbing properties, enables pain-free physiological movements; it also supplies nutrients to the cartilage. The \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003eThe contained sodium hyaluronate is a salt of hyaluronic acid.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eIndications\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePain and limitation of joint mobility in degenerative changes of the knee joint and other synovial joints, including osteoarthritis.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eContraindications\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used in patients\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- with known hypersensitivity to any of the components\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003e- with inflammation in the joint\u003cbr\u003e- with septic arthritis\u003cbr\u003e- with skin infections or skin diseases in the injection area\u003cbr\u003e- with natural or medication-induced coagulation disorders such as hemophilia or under use\u003c\/span\u003e\u003cspan\u003euse of anticoagulants such as Marcumar (phenprocoumon) or Coumadin (warfarin)\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eSince there are no clinical data on the use of hyaluronic acid in children, pregnant or breastfeeding women, use in these patients is not recommended.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003ePrecautions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSince septic arthritis can be a serious complication of treatment, please observe all precautions usually necessary for surgical procedures. Injections of the hydrogel must be administered directly into the joint cavity; injections into blood vessels and surrounding tissue must be avoided. Do not use if the prefilled syringe or sterile packaging is damaged.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan style=\"font-size: 0.875rem;\"\u003eThe opened product must not be resterilized, resealed, or reused. It is intended for use by a single patient at a single treatment session.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003ePossible side effects\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eNo adverse effects were observed in biocompatibility tests with the product. In the treated\u003c\/span\u003e\u003cspan\u003e- affected joint, local symptoms such as pain, redness, warmth, and swelling may occur. \u003c\/span\u003e\u003cspan\u003eThese symptoms can be reduced if the treated area is cooled with an ice pack for 5 to 10 minutes after injection. During the first days of treatment, the simultaneous oral intake of pain and anti-inflammatory medications (NSAIDs) may be beneficial. In cases of intense \u003c\/span\u003e\u003cspan\u003eIf pain or inflammation occurs, treatment should be discontinued. Treatment of adverse reactions should only be carried out under the supervision of the attending physician. Immediately after the injection, strenuous physical activity should be avoided and other instructions from the doctor should be followed. Medical personnel should inform the patient\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003e- about possible adverse events related to the product.\u003cbr\u003e- that the patient must report any adverse event or complication to a doctor. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003ePharmacological and chemical interactions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eSo far, there are no data on the incompatibility of the product with other solutions for intra-articular use.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eThere is a chemical incompatibility between sodium hyaluronate and quaternary ammonium compounds. \u003c\/span\u003e\u003cspan\u003esuch as benzalkonium chloride, which can lead to crystalline precipitation. Therefore, this product must never come into contact with surgical instruments or other products that contain these, or with \u003c\/span\u003e\u003cspan\u003eSolutions containing quaternary ammonium compounds as biocidal preservatives. \u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eDosage, type, and duration of use\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe prefilled syringe is to be removed from its packaging. The protective cap is to be removed from the Luer-Lock thread. A suitable sterile injection needle is to be screwed onto the syringe. The use of a single-use needle is recommended. Air should be evacuated from the needle before injection. The skin area intended for injection must be cleaned with an appropriate topical antiseptic. In the case of joint effusion, it is recommended that solutions containing quaternary ammonium compounds as biocidal preservatives be rinsed before injection. \u003c\/span\u003e\u003cspan\u003eKD Intra-Articular\u003c\/span\u003e\u003cspan\u003e® \u003c\/span\u003e\u003cspan\u003eGel \u003c\/span\u003e\u003cspan\u003einitially reduce the effusion by aspiration and examine it for bacterial etiology. The hydrogel can be injected 1 to 5 times at intervals determined by the physician. \u003c\/span\u003e\u003cspan\u003eInjected intra-articularly at intervals. The beneficial effects of a treatment last at least 6 months. Treatment cycles can be repeated if necessary.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eDepending on the fill volume, several joints of a patient can be treated simultaneously. Unused product must be disposed of.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDosage form\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eA box with one prefilled syringe of 1 ml - 4.8 ml.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eDurability\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product must not be used after the expiration date. The expiration date (month\/year) is printed on the \u003c\/span\u003e\u003cspan\u003eSyringe blister and printed on the carton.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eStorage instructions\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eThe product should be stored dry between 2° and 25°C and protected from light and impact in the original packaging. Accordingly, warning symbols on the packaging must be observed.\u003cbr\u003eKeep the product out of reach of children.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eRecommended user group\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003c\/span\u003e\u003cspan\u003eIntended exclusively for use by physicians.\u003cbr\u003eFor single use only. Do not resterilize. Do not use syringes, needles, or hydrogel from open or damaged packaging or attempt to reseal packaging.\u003cbr\u003eSyringe content is non-toxic and non-flammable.\u003cbr\u003e\u003c\/span\u003e\u003cspan\u003eWhen using a product from damaged packaging or reusing with other \u003c\/span\u003e\u003cspan\u003epatients or the same patient at a different time are the intended properties and the \u003c\/span\u003e\u003cspan\u003eSterility is not guaranteed. Otherwise, possible transmission of material contamination and pathogens \u003c\/span\u003e\u003cspan\u003efrom the environment, the clinical area, or (other) patients could lead to health complications \u003c\/span\u003e\u003cspan\u003elead to. Resealing or resterilization does not constitute an allowed or guaranteed restoration of \u003c\/span\u003e\u003cspan\u003eusable condition.\u003cbr\u003eUnused syringes and their contents are not infectious and can be disposed of before or after the expiration date, observing national and local regulations. Used syringes and needles must be treated as epidemiologically hazardous waste, and national and local regulations for safe use and disposal must be followed.\u003c\/span\u003e\u003c\/p\u003e\n\u003cdiv class=\"page\" title=\"Page 1\"\u003e\n\u003cdiv class=\"section\"\u003e\n\u003cdiv class=\"layoutArea\"\u003e\n\u003cdiv class=\"column\"\u003e\n\u003cp\u003e\u003cspan\u003eStatus of information 05\/2021\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e\n\u003c\/div\u003e","brand":"ALBOMED GmbH","offers":[{"title":"Default Title","offer_id":47355879358804,"sku":"107","price":74.9,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0786\/8756\/8212\/files\/albomed-innoryos-albomed-gmbh-gelenkspritzen-stakonmed-473622.jpg?v=1772213397"}],"url":"https:\/\/stakonmed.at\/en\/collections\/albomed.oembed","provider":"StakonMed","version":"1.0","type":"link"}