ORTHOFLEX® tendon//Restore mobility in damaged tendon
Prefilled syringes|
Number one in sprained ankle treatment
ORTHOFLEX tendon® is injectable prefilled syringe 40mg/2ml natural solution of highly purified sodium hyaluronate obtained by biofermentation devoid of animal protein + 10 mg mannitol , a free radical scavenger which help to stabilize the chains of sodium hyaluronate.
Sodium Hyaluronate 40 mg/2ml + 10mg mannitol
Description
Treatment of Painful Tendinopathy
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ORTHOFLEX tendon® is a viscoelastic gel for peritendinous or intrasheath injections.
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ORTHOFLEX tendon® is an injectable prefilled syringe 40mg/2ml natural solution of highly purified sodium hyaluronate obtained by biofermentation devoid of animal protein + 10 mg mannitol , a free radical scavenger which help to stabilize the chains of sodium hyaluronate.
Effects
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Acts as a lubricant when applied into the tendon sheath or peritendinously.
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Enhance tendon gliding effect and reduce adhesion.
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Prevents the free passage of inflammatory cell and molecules through the tendon sheath due to its macromolecular meshwork.
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Promotes tendon recovery and would healing process.
Precautions
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ORTHOFLEX tendon® should be instilled accurately into tendon sheath or around the affected tendon if necessary under imaging control, avoid nerve lesions and injections into blood vessels.
Indications
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For the treatment of pain and restricted mobility in tendon disorders.
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Ankle and Foot
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achilles tendinopathy
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posterior tibial tendinopathy
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peroneal tendinopaty
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Shoulder- rotator cuff tendinopathy
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Elbow- lateral and medial epicondylalgia
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Knee – patellar tendinopathy
ORTHOFLEX tendon® should be administred once a week for total of 2 injections.
Caracteristics:
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Treatment of tendon disorders
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2 ml prefilled syringe for single use
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Sodium hyaluronate 2%( 40mg/2ml)+ mannitol( 10mg)
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Molecular weight- 3000kDa
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Duration on effects – 6 month
Quality:
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ORTHOFLEX tendon® is produced according to Good Manufacturing Practice (GMP) and ISO13485 being certified as a system with high quality ingredients, CE marked medical device being in accordance with the European Directive 93/42/EE.