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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/2023/000462_f6899d34faf34550e361aff1bf7645c8_20c1b59e5739d74e4e9f1901972300a7. This device is marketed under the brand name PEEK Interference Screw. The license holder is Morulaa Health Tech 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
Meniscal Repair System
UID: IMP/MD/2023/000462_f6899d34faf34550e361aff1bf7645c8_20c1b59e5739d74e4e9f1901972300a7

Brand Name

PEEK Interference Screw

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Meniscal Repair System is intended for use as a suture retention device to facilitate percutaneous or endoscopic soft tissue procedures. The system is indicated for use in meniscal repairs and allograft transplant procedures. The system is intended to be used for anchoring the allograft to the meniscal rim during allograft transplant procedures.

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