Pure Global

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_0f4f2c3aa69f14fa16ad3235f1118a1a. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
FIXATION SCREW
UID: IMP/MD/2019/000479_d82ed17766d3c3883c6b7ede9439df65_0f4f2c3aa69f14fa16ad3235f1118a1a

Brand Name

TWINFIX ULTRA Ti

Device Class

Class C

Approving Authority

CDSCO

Product Information

RCI Fixation Screws are used for interference fixation of bone-tendon-bone or soft tissue grafts in anterior or posterior cruciate ligament reconstruction

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing