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Nonabsorbable Synthetic Surgical Mesh(PROLENE* Hernia System) - India CDSCO Medical Device Registration

Nonabsorbable Synthetic Surgical Mesh(PROLENE* Hernia System) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000012_966dd0db652f7ca5676e95734adaf902_d7a7104b7947854b6012c2aa403c4c9a. This device is marketed under the brand name BLACK BRAIDED SILK. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class C. 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 C
Nonabsorbable Synthetic Surgical Mesh(PROLENE* Hernia System)
UID: MFG/MD/2020/000012_966dd0db652f7ca5676e95734adaf902_d7a7104b7947854b6012c2aa403c4c9a

Brand Name

BLACK BRAIDED SILK

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

The PROLENE* (BLACK BRAIDED SILK) Hernia System is indicated for the repair of inguinal (BLACK BRAIDED SILK) and abdominal wall hernia defects

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