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FIXATION SCREW - India CDSCO Medical Device Registration

FIXATION SCREW is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000479_d82ed17766d3c3883c6b7ede9439df65_50641936f1a13cc53715707ad9fe7dff. This device is marketed under the brand name TWINFIX ULTRA Ti. The license holder is Smith & Nephew Healthcare Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class C
FIXATION SCREW
UID: IMP/MD/2019/000479_d82ed17766d3c3883c6b7ede9439df65_50641936f1a13cc53715707ad9fe7dff

Brand Name

TWINFIX ULTRA Ti

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Smith & Nephew SOFTSILK Screws are used for interference fixation of bone-tendon-bone or soft tissue grafts in anteriorcruciate ligament reconstruction

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