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Coronary Artery Bypass Graft - India CDSCO Medical Device Registration

Coronary Artery Bypass Graft is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000012_f95248b80b7bdad7c7c6d4cfc24c3be2_b43ccd168cec0a7c9e194b8e5282666c. 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
Coronary Artery Bypass Graft
UID: MFG/MD/2020/000012_f95248b80b7bdad7c7c6d4cfc24c3be2_b43ccd168cec0a7c9e194b8e5282666c

Brand Name

PROLENE*

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Surgical Procedures relared to Coronary Artery Bypass

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