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Bioinductive Implant - India CDSCO Medical Device Registration

Bioinductive Implant is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000479_292b5124345b9407fba2b02959ab284a_9cbdf74eb643084c29d7cd971356d7bc. This device is marketed under the brand name HEALICOIL Knotless REGENESORB. The license holder is Smith & Nephew Healthcare Pvt. Ltd, 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
Bioinductive Implant
UID: IMP/MD/2019/000479_292b5124345b9407fba2b02959ab284a_9cbdf74eb643084c29d7cd971356d7bc

Brand Name

HEALICOIL Knotless REGENESORB

Device Class

Class D

Approving Authority

CDSCO

Product Information

The REGENETEN Bioinductive Implant is indicated for the management and protection of rotator cuff tendon injuries in which there has been no substantial loss of tendon tissue.

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