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Hernia Kit - India CDSCO Medical Device Registration

Hernia Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000012_adb68e26ed208ccaac3f4e2fac30c1e3_67a34925d3053335700c3c24c1673cbc. This device is marketed under the brand name PROLENE*. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.

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
Hernia Kit
UID: MFG/MD/2020/000012_adb68e26ed208ccaac3f4e2fac30c1e3_67a34925d3053335700c3c24c1673cbc

Brand Name

PROLENE*

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Surgical Procedures relared to Hernia Surgery

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