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Meniscal Repair System - India CDSCO Medical Device Registration

Meniscal Repair System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000335_f6899d34faf34550e361aff1bf7645c8_0426f0e2f3449f9301c92f68164936cf. This device is marketed under the brand name Healix Advance Knotless PEEK Anchor. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. 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 D
Meniscal Repair System
UID: IMP/MD/2019/000335_f6899d34faf34550e361aff1bf7645c8_0426f0e2f3449f9301c92f68164936cf

Brand Name

Healix Advance Knotless PEEK Anchor

Device Class

Class D

Approving Authority

CDSCO

Product Information

The OMNISPAN System is intended for use in the arthroscopic fixation of soft tissue procedures such as meniscal repair

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