Ventral Patch - India CDSCO Medical Device Registration

Ventral Patch is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000141_48b71aa46abdf013180d0640a105e0ba_68aa6f7c6c561e2c022a0bf5adf5958c. 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

Ventral Patch

UID: IMP/MD/2020/000141_48b71aa46abdf013180d0640a105e0ba_68aa6f7c6c561e2c022a0bf5adf5958c

Brand Name

Proceed Ventral Patch

License Holder

Johnson & Johnson Private Limited

Device Class

Class D

Approving Authority

CDSCO

Product Information

PROCEED™ Ventral Patch is indicated for the open repair of ventral hernias that require the addition of a reinforcing material to obtain the desired surgical result

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Surgical mesh

Brand: Proceed Ventral Patch

Johnson & Johnson Private Limited

Ventral Patch - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

Surgical mesh

Mesh

Mesh

Mesh

Mesh

Sutures

Sutures

Sutures

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Coronary Artery Bypass Graft

NON-STERILE NON-ABSORBABLE SURGICAL SUTURE U.S.P.

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NON ABSORBABLE SURGICAL SUTURE U. S. P.

NON ABSORBABLE SURGICAL SUTURE U. S. P.

NON ABSORBABLE SURGICAL SUTURE U. S. P.

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