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Sinovial Siringa Intra-Articolare 16 Acido Ialuronico 0,8% 2ml 3 Pezzi
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Special Price €54.15 -53% Regular Price €114.30
The price was: €54.15
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Description Sinovial Siringa Intra-Articolare 16 Acido Ialuronico 0,8% 2ml 3 Pezzi
SINOVIAL 16 2 ml
0.8% 16 mg / 2 ml
Description
Synovial fluid substitute , which allows you to restore the properties physiological and rheological of the arthritic joints. This therapeutic action is explained by the particular characteristics of the hyaluronic acid used. The hyaluronic acid contained in SINOVIAL 16 2 ml, obtained by fermentation and not chemically modified, has an excellent tolerability. Restoring the properties viscoelastic synovial fluid, SINOVIAL 16 2 ml reduces pain and restores mobility; articular and tendon.
SINOVIAL 16 2 ml acts only at the level of the area where it is injected, without exerting any systemic action. The improvement is; immediate: already; after the first injection, the global WOMAC index decreases and from the third injection the decrease becomes statistically significant.
Indicated in case of acute and chronic tendinopathies and / or associated with disabilities. joint and in the tendon repair process, including after surgery. SINOVIAL 16 2 ml È a medical device designed to integrate the synovial fluid, allowing to restore its properties; physiological and rheological of the arthritic joints and tendons. In the joint SINOVIAL 16 2 ml reduces pain and promotes the recovery of mobility; joint and associated tendon, acting only in the cavity; synovial into which it is injected, without exerting any systemic action. SINOVIAL 16 2 ml also, thanks to its lubricating and viscoelastic characteristics, acts at the level of the tendon sheath, where it improves the sliding of the tendon (& ldquo; Tendon gliding & rdquo;) and the physiological processes of healing / repair, thus preventing the formation of adhesions in post-operative courses.
Modality À of use
Aspirate any joint effusion before proceeding with the injection.
Carefully unscrew the cap of the seal, keeping the 'Luer Lock' locking collar firmly between your fingers and paying particular attention be careful to avoid contact with the opening. Insert the needle into the syringe Luer Lock type locking collar (needle diameter between 18 and 22G) by screwing it firmly, until a slight pressure is felt to ensure a watertight seal and prevent liquid leakage during administration, keeping the 'Luer Lock' locking collar firmly between the fingers.
Inject SINOVIAL 16 2 ml at room temperature and in conditions of strict asepsis, inside the synovial space of the joint or in the tendon sheath / peri-tendon area , depending on the need À medical identified.
Components
0.8% hyaluronic acid, highly purified sodium salt (molecular weight between 800 and 1,200 KDalton), sodium chloride, phosphate sodium, water for injections.
Warnings
SINOVIAL 16 2 ml pu Ò be injected by a physician only.
The contents of the pre-filled syringe are injected. sterile.
The syringe is; packed in a sealed blister. The outer surface of the syringe is not sterile.
Do not use after the expiry date stated on the package.
Do not use if the packaging is; open or damaged.
The injection site must be on healthy skin.
Do not inject by the vascular route. Do not inject outside the cavity; joint, synovial tissue or joint capsule. Do not administer in the presence of abundant intra-articular effusion. Do not re-sterilize. The device is intended for single use only. Do not reuse to avoid any risk of contamination.
Once opened, it must be used immediately and discarded after use.
Keep out of the reach and sight of children.
After intra-articular or synovium injection tendon, advise the patient to avoid all activities intense physical activity and to resume normal activities; only after a few days.
The possible presence of an air bubble does not affect the characteristics of the product.
Do not mix SINOVIAL with disinfectants such as quaternary ammonium salts or chlorhexidine since can Ò form a precipitate.
The extra-articular infiltration of SINOVIAL 16 2 ml can Ò locally cause undesirable effects. While using SINOVIAL 16 2 ml, symptoms such as pain, warmth, redness or swelling may appear at the injection site. These secondary manifestations can be alleviated by applying ice to the treated area. They usually disappear after a short time. The physician must ensure that patients inform him of any undesirable effects occurring after treatment.
SINOVIAL 16 2 ml must not be injected in the presence of an infected or severely inflamed joint, or if the patient has a skin condition or disease. infection in the injection site area.
The product should not be used in case of hypersensitivity known to sodium hyaluronate or to the other components.
To date there are no known interactions between SINOVIAL 16 2 ml and other drugs.
Do not mix with disinfectants such as quaternary ammonium salts or chlorhexidine since can Ò precipitate.
It should not be injected if there is an infected or severely inflamed joint or if the patient has a skin condition or infection in the injection site area. The product should not be used in case of hypersensitivity note to sodium hyaluronate or other components.
SINOVIAL 16 2 ml pu Ò be injected only by a doctor.
Storage
Store at room temperature and in any case below 25 ° C and away from heat sources. Do not freeze.
Validity À unopened: 36 months.
Format
Packs of 3 pre-filled syringes (16.0 mg of hyaluronic acid sodium salt in 2 ml of chloride buffered saline sodium) and 3 needles 21 G x 1 & frac12; ' (0.8 x 40 mm).
Cod. 6000001295
Synovial fluid substitute , which allows you to restore the properties physiological and rheological of the arthritic joints. This therapeutic action is explained by the particular characteristics of the hyaluronic acid used. The hyaluronic acid contained in SINOVIAL 16 2 ml, obtained by fermentation and not chemically modified, has an excellent tolerability. Restoring the properties viscoelastic synovial fluid, SINOVIAL 16 2 ml reduces pain and restores mobility; articular and tendon.
SINOVIAL 16 2 ml acts only at the level of the area where it is injected, without exerting any systemic action. The improvement is; immediate: already; after the first injection, the global WOMAC index decreases and from the third injection the decrease becomes statistically significant.
Indicated in case of acute and chronic tendinopathies and / or associated with disabilities. joint and in the tendon repair process, including after surgery. SINOVIAL 16 2 ml È a medical device designed to integrate the synovial fluid, allowing to restore its properties; physiological and rheological of the arthritic joints and tendons. In the joint SINOVIAL 16 2 ml reduces pain and promotes the recovery of mobility; joint and associated tendon, acting only in the cavity; synovial into which it is injected, without exerting any systemic action. SINOVIAL 16 2 ml also, thanks to its lubricating and viscoelastic characteristics, acts at the level of the tendon sheath, where it improves the sliding of the tendon (& ldquo; Tendon gliding & rdquo;) and the physiological processes of healing / repair, thus preventing the formation of adhesions in post-operative courses.
Modality À of use
Aspirate any joint effusion before proceeding with the injection.
Carefully unscrew the cap of the seal, keeping the 'Luer Lock' locking collar firmly between your fingers and paying particular attention be careful to avoid contact with the opening. Insert the needle into the syringe Luer Lock type locking collar (needle diameter between 18 and 22G) by screwing it firmly, until a slight pressure is felt to ensure a watertight seal and prevent liquid leakage during administration, keeping the 'Luer Lock' locking collar firmly between the fingers.
Inject SINOVIAL 16 2 ml at room temperature and in conditions of strict asepsis, inside the synovial space of the joint or in the tendon sheath / peri-tendon area , depending on the need À medical identified.
Components
0.8% hyaluronic acid, highly purified sodium salt (molecular weight between 800 and 1,200 KDalton), sodium chloride, phosphate sodium, water for injections.
Warnings
SINOVIAL 16 2 ml pu Ò be injected by a physician only.
The contents of the pre-filled syringe are injected. sterile.
The syringe is; packed in a sealed blister. The outer surface of the syringe is not sterile.
Do not use after the expiry date stated on the package.
Do not use if the packaging is; open or damaged.
The injection site must be on healthy skin.
Do not inject by the vascular route. Do not inject outside the cavity; joint, synovial tissue or joint capsule. Do not administer in the presence of abundant intra-articular effusion. Do not re-sterilize. The device is intended for single use only. Do not reuse to avoid any risk of contamination.
Once opened, it must be used immediately and discarded after use.
Keep out of the reach and sight of children.
After intra-articular or synovium injection tendon, advise the patient to avoid all activities intense physical activity and to resume normal activities; only after a few days.
The possible presence of an air bubble does not affect the characteristics of the product.
Do not mix SINOVIAL with disinfectants such as quaternary ammonium salts or chlorhexidine since can Ò form a precipitate.
The extra-articular infiltration of SINOVIAL 16 2 ml can Ò locally cause undesirable effects. While using SINOVIAL 16 2 ml, symptoms such as pain, warmth, redness or swelling may appear at the injection site. These secondary manifestations can be alleviated by applying ice to the treated area. They usually disappear after a short time. The physician must ensure that patients inform him of any undesirable effects occurring after treatment.
SINOVIAL 16 2 ml must not be injected in the presence of an infected or severely inflamed joint, or if the patient has a skin condition or disease. infection in the injection site area.
The product should not be used in case of hypersensitivity known to sodium hyaluronate or to the other components.
To date there are no known interactions between SINOVIAL 16 2 ml and other drugs.
Do not mix with disinfectants such as quaternary ammonium salts or chlorhexidine since can Ò precipitate.
It should not be injected if there is an infected or severely inflamed joint or if the patient has a skin condition or infection in the injection site area. The product should not be used in case of hypersensitivity note to sodium hyaluronate or other components.
SINOVIAL 16 2 ml pu Ò be injected only by a doctor.
Storage
Store at room temperature and in any case below 25 ° C and away from heat sources. Do not freeze.
Validity À unopened: 36 months.
Format
Packs of 3 pre-filled syringes (16.0 mg of hyaluronic acid sodium salt in 2 ml of chloride buffered saline sodium) and 3 needles 21 G x 1 & frac12; ' (0.8 x 40 mm).
Cod. 6000001295
