Hernia System - India CDSCO Medical Device Registration

Hernia System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000141_50271011a7811d9353515b5b3b09c264_83dbc106691479823d116f5c7f8681c0. 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.

Free Database

CDSCO Registered

Class Class D

Hernia System

UID: IMP/MD/2020/000141_50271011a7811d9353515b5b3b09c264_83dbc106691479823d116f5c7f8681c0

Brand Name

Proceed Ventral Patch

License Holder

Johnson & Johnson Private Limited

Device Class

Class D

Approving Authority

CDSCO

Product Information

This product is indicated for open repair of abdominal wall hernia defects

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Surgical mesh

Brand: Proceed Ventral Patch

Johnson & Johnson Private Limited

Hernia System - 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

Ventral Patch

C-Section Kit

Coronary Artery Bypass Graft

Coronary Artery Bypass Graft

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

Coronary Artery Bypass Graft(ETHICON* CABG KIT)

NON ABSORBABLE SURGICAL SUTURE U. S. P.

NON ABSORBABLE SURGICAL SUTURE U. S. P.

NON ABSORBABLE SURGICAL SUTURE U. S. P.

ABHY-ADV KIT

Hernia Kit