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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/2023/000528_76dd9d462e9ff1c1fe9da2d50679fb98_ec517a142250f98c3e69623232ea7039. This device is marketed under the brand name SEGURO/ULTIMA/MAGNA. The license holder is Seguro Lifesciences, and it is classified as Device Class Class B. The approving authority is Solan(BBN).

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/2023/000528_76dd9d462e9ff1c1fe9da2d50679fb98_ec517a142250f98c3e69623232ea7039

Brand Name

SEGURO/ULTIMA/MAGNA

License Holder

Seguro Lifesciences

Device Class

Class B

Approving Authority

Solan(BBN)

Product Information

Manifold is indicated for fluid flow directional control and for providing access ports for administration of solutions. Typical uses include pressure monitoring, intravenous fluid administration and transfusion

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