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Surgical mesh - India CDSCO Medical Device Registration

Surgical mesh is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000141_ec9f34f0158776e133d6fe611ee5dc9e_518863457e26cf6fa277aa78e71c783c. This device is marketed under the brand name Proceed Ventral Patch. 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
Surgical mesh
UID: IMP/MD/2020/000141_ec9f34f0158776e133d6fe611ee5dc9e_518863457e26cf6fa277aa78e71c783c

Brand Name

Proceed Ventral Patch

Device Class

Class D

Approving Authority

CDSCO

Product Information

PROCEED™SurgicalMeshisindicatedfortherepairofabdominalwallherniasthatrequiretheadditionofareinforcingmaterialtoobtainthede siredsurgicalresult.

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