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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/2023/000061_76dd9d462e9ff1c1fe9da2d50679fb98_abbb455ead773fde0f702b0082f93329. This device is marketed under the brand name GEEMED. The license holder is GEEMED HEALTHCARE, and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.

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/2023/000061_76dd9d462e9ff1c1fe9da2d50679fb98_abbb455ead773fde0f702b0082f93329

Brand Name

GEEMED

License Holder

GEEMED HEALTHCARE

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

It is intended to use in diagnostic and interventional applications to control or direct fluid flow between tubing, catheters, or other devices

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