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Hernia Repair Device - India CDSCO Medical Device Registration

Hernia Repair Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000017_eaa520c9eabcb94e8eae6b2799b5013f_505463694a6301a9679fe356345207cf. 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
Hernia Repair Device
UID: IMP/MD/2022/000017_eaa520c9eabcb94e8eae6b2799b5013f_505463694a6301a9679fe356345207cf

Brand Name

Ventralight ST Mesh

Device Class

Class C

Approving Authority

CDSCO

Product Information

BARD 3DMAX mesh is indicated to reinforce soft tissue where weakness exists, e.g., for repair of hernia and chest wall defects

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