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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_9efb1f5fae1be7cc4291d83c030e4ba3. 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_9efb1f5fae1be7cc4291d83c030e4ba3

Brand Name

CAPIOX FX

Device Class

Class B

Approving Authority

CDSCO

Product Information

The CAPIOX RX is a single-use sterile device that substitutes a patientโ€™s internal organ. This is a membrane oxygenator used as a part of heart-lung machine to oxygenate blood and remove carbon dioxide from blood during open-heart surgery.

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