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MAGICL CEA - India CDSCO Medical Device Registration

MAGICL CEA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000403_ff57717f2927cfc59da4f558c4c3a7dd_c3ccaab19f9a53598f946bddb2822474. 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 CEA
UID: IMP/IVD/2019/000403_ff57717f2927cfc59da4f558c4c3a7dd_c3ccaab19f9a53598f946bddb2822474

Brand Name

CLIA

Device Class

Class B

Approving Authority

CDSCO

Product Information

MAGICL CEA (CLIA) is intended for the in vitro quantitative determination of carcinoembryonic antigen (CLIA) in human serum or plasma. Clinically, it is mainly used for the observation of the treatment efficacy, prognosis and recurrence monitoring in patients with malignant tumors

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