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Anchor with Suture - India CDSCO Medical Device Registration

Anchor with Suture is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000335_ebf5d2138c2100d19465ca5e1245eb84_51fb19878146dcd47a320bab93bc7a69. 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
Anchor with Suture
UID: IMP/MD/2019/000335_ebf5d2138c2100d19465ca5e1245eb84_51fb19878146dcd47a320bab93bc7a69

Brand Name

Healix Advance Knotless PEEK Anchor

Device Class

Class D

Approving Authority

CDSCO

Product Information

"The GRYPHON Anchor with PROKNOT Technology is intended for: Shoulder: Bankart Repair, SLAP Lesion Repair, Capsular Shift or Capsulolabral Reconstruction Hip: Capsular Repair, Acetabular Labral Repair."

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