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Extra-corporeal Membrane Oxygenator - India CDSCO Medical Device Registration

Extra-corporeal Membrane Oxygenator is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000613_a71c9a53e4d25cd07c15fe5f5958e02c_e9baed74733281f92a765c4844d0229e. This device is marketed under the brand name CAPIOX FX. The license holder is M/s. Terumo India Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

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
Extra-corporeal Membrane Oxygenator
UID: IMP/MD/2022/000613_a71c9a53e4d25cd07c15fe5f5958e02c_e9baed74733281f92a765c4844d0229e

Brand Name

CAPIOX FX

Device Class

Class B

Approving Authority

CDSCO

Product Information

The CAPIOX FX is an extracorporeal membrane oxygenator used as a part of heart-lung machine to remove carbon dioxide and foreign substances from blood during open-heart surgery

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