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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/2021/000291_76dd9d462e9ff1c1fe9da2d50679fb98_7c4ae5a6e4eed723a29084ee3e1e7a45. The license holder is STERILE WORLD TECHNOLOGOIES LLP., and it is classified as Device Class Class B. The approving authority is Aurangabad Division.

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/2021/000291_76dd9d462e9ff1c1fe9da2d50679fb98_7c4ae5a6e4eed723a29084ee3e1e7a45

Device Class

Class B

Approving Authority

Aurangabad Division

Product Information

Manifolds are intended to serve as flow control and delivery devices for I.V fluids injection to the patient's vascular system

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