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Manifold - India CDSCO Medical Device Registration

Manifold is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2021/000243_76dd9d462e9ff1c1fe9da2d50679fb98_ad610343b450697521089c5a7edb08ef. This device is marketed under the brand name AngiX. The license holder is B L Lifesciences Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.

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 B
Manifold
UID: MFG/MD/2021/000243_76dd9d462e9ff1c1fe9da2d50679fb98_ad610343b450697521089c5a7edb08ef

Brand Name

AngiX

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

Manifold is a hand-controlled device used during the injection of contrast media during angiography procedure

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