SYNOLIS VA SODIUM VISCO IALURONATE & SORBITOL ANTALCIC Medical device CE Class III. Synolis VA is indicated to reduce pain and improve mobilitàdell'articolazione knee and other synovial joints affected daalterazioni degenerative and traumatic. Synolis VA is a soluzioneviscoelastica sterile, apyrogenic and isotonic with a basis of sodium hyaluronate dissolved A LIVE buffered saline. Sodium hyaluronate content in questodispositivo doctor for injection by the intra-articular is obtained mediantefermentazione bacterial, it has a high concentration (2%) and a high pesomolecolare with average weight of 2,000,000 Daltons in sterilized solution. The forteconcentrazione and the high molecular weight of sodium hyaluronate, associated allapresenza of an excipient (sorbitol) which limits degradation and capacitàdella viscoelastic solution to lubricate the joints and to absorb impacts, simulating the rheological properties of the synovial fluid, determinanol 'effectiveness of this product in the treatment of osteoarthritis. Synolis V-Aagisce restoring the physiological and rheological fluid sinovialeaffetto from osteoarthritis, making it possible to reduce pain and its way of fastidiocosì as improve joint mobility. Synolis VA is presentain glass syringe pre-filled with 2 ml. The syringe is contained in a single casing diprotezione sterilized. There are two types of packaging: box of 1 or 3 syringes containing directions for use and a leaflet. Dosage and method of administration Synolis VA must be injected in the joint to a doctor who specializes ininiezioni intraarticular. Draw off payments before injecting Synolis. Synolis VA must be injected at room temperature. Perform a strict aseptic injection site. Use a needle of suitable length and dimension (it is recommended that 18 to 21 G, 2 "). Firmly tighten the needle to the luer lock syringe. Inject only within the joint cavity. In cases of knee arthritis it is advisable to administer Synolis VA follo
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