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Mesh - India CDSCO Medical Device Registration

Mesh is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000017_710fdb6adb881b408116ef95335e1961_cf3ccaaa7bea9629a9bc47280d34d320. This device is marketed under the brand name Ventralight ST Mesh. The license holder is Becton Dickinson India Private Limited, 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
Mesh
UID: IMP/MD/2022/000017_710fdb6adb881b408116ef95335e1961_cf3ccaaa7bea9629a9bc47280d34d320

Brand Name

Ventralight ST Mesh

Device Class

Class C

Approving Authority

CDSCO

Product Information

Phasix Mesh is indicated to reinforce soft tissue where weakness exists in patients undergoing plastic and reconstructive surgery, or for use in procedures involving soft tissue repair, such as the repair of hernia or other fascial defects that require the addition of a reinforcing or bridging material to obtain the desired surgical result

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