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Suture - India CDSCO Medical Device Registration

Suture is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000335_bf0eb4c378858755c91f83864f5c5b8e_d0bc96cdd532210684c74f026602430b. 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
Suture
UID: IMP/MD/2019/000335_bf0eb4c378858755c91f83864f5c5b8e_d0bc96cdd532210684c74f026602430b

Brand Name

Healix Advance Knotless PEEK Anchor

Device Class

Class D

Approving Authority

CDSCO

Product Information

Orthocord Suture is indicated for use in general soft tissue approximation, and/or ligation, including Orthopedic procedures. It is not indicated for cardiovascular or neurological procedures

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