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Graft Preparation System - India CDSCO Medical Device Registration

Graft Preparation System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000003_f37708d962ef99a171cc1a67363e14de_8bef16fb1e094cf381fc99f578d5449d. This device is marketed under the brand name GII 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
Graft Preparation System
UID: IMP/MD/2019/000003_f37708d962ef99a171cc1a67363e14de_8bef16fb1e094cf381fc99f578d5449d

Brand Name

GII Anchor

Device Class

Class D

Approving Authority

CDSCO

Product Information

The SPEEDTRAP suture construct is indicated for use in soft tissue approximation in orthopedic procedures.

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