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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/2021/000444_9dbaa6e6cafc0d78c8d831d11106f356_909d7dbeb9e0f64f7294dc8f3e47e33e. The license holder is Angstrom Biotech Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Rajasthan.

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/2021/000444_9dbaa6e6cafc0d78c8d831d11106f356_909d7dbeb9e0f64f7294dc8f3e47e33e

Device Class

Class B

Approving Authority

Rajasthan

Product Information

lt is intended for providing multiple ports for administration of solution with directional control

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