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MAGICL AFP - India CDSCO Medical Device Registration

MAGICL AFP is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000403_fef5ca0e7dffb44c5ebc1cec0c02dedc_8e235aa0b1f5d1ded34599baba451a25. This device is marketed under the brand name CLIA. The license holder is M/s. Reckon Diagnostics 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
MAGICL AFP
UID: IMP/IVD/2019/000403_fef5ca0e7dffb44c5ebc1cec0c02dedc_8e235aa0b1f5d1ded34599baba451a25

Brand Name

CLIA

Device Class

Class B

Approving Authority

CDSCO

Product Information

MAGICL AFP (CLIA) is intended for the in vitro quantitative determination of alphafetoprotein (CLIA) in human serum and plasma. Clinically, it is mainly used for the auxiliary diagnosis, curative effect and prognosis observation of primary liver cancer

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