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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/2020/000113_9dbaa6e6cafc0d78c8d831d11106f356_18f6e3017bb5b8bb818ae700c8dc6ba6. This device is marketed under the brand name SURETECH. The license holder is Suretech Medical Inc, and it is classified as Device Class Class B. The approving authority is Greater Mumbai 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/2020/000113_9dbaa6e6cafc0d78c8d831d11106f356_18f6e3017bb5b8bb818ae700c8dc6ba6

Brand Name

SURETECH

License Holder

Suretech Medical Inc

Device Class

Class B

Approving Authority

Greater Mumbai Division

Product Information

INDICATED FOR FLUID FLOW DIRECTION CONTROL AND PROVIDING ACCESS PORT/PORTS FOR ADMINISTRATION OF A SOLUTION

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