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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/2023/000289_76dd9d462e9ff1c1fe9da2d50679fb98_06fe9c3636b87ae1696d3996cffb8d36. This device is marketed under the brand name ClearNeedle. The license holder is Newtech Medical Devices Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Haryana.

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/2023/000289_76dd9d462e9ff1c1fe9da2d50679fb98_06fe9c3636b87ae1696d3996cffb8d36

Brand Name

ClearNeedle

Device Class

Class B

Approving Authority

Haryana

Product Information

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

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