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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/2020/000048_76dd9d462e9ff1c1fe9da2d50679fb98_2c228141650b7e0a33545a5dc5273703. This device is marketed under the brand name CUSTOMIZED PACK. The license holder is M/S Spectrum Med Tech Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Gujarat.

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/2020/000048_76dd9d462e9ff1c1fe9da2d50679fb98_2c228141650b7e0a33545a5dc5273703

Brand Name

CUSTOMIZED PACK

Device Class

Class B

Approving Authority

Gujarat

Product Information

Indicated for fluid flow directional control and providing access port/ports for administration of a solution

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