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Clinical Chemistry Analyser - India CDSCO Medical Device Registration

Clinical Chemistry Analyser is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_b00f085e1cc234f89e482133089a1746_df3a86072a69c286b2cc8861664a6d90. This device is marketed under the brand name HumaCLIA 150 . The license holder is M/s Stedman Pharmaceuticals Pvt. Ltd., and it is classified as Device Class Class A. 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 A
Clinical Chemistry Analyser
UID: IMP/IVD/2019/000206_b00f085e1cc234f89e482133089a1746_df3a86072a69c286b2cc8861664a6d90

Brand Name

HumaCLIA 150

Device Class

Class A

Approving Authority

CDSCO

Product Information

The HumaLyzer 4000 is an open in-vitro diagnostic chemistry analyzer/photometer for testing of routine clinical chemistry and turbidimetric parameters. in-vitro diagnostic photometer for testing of routine clinical chemistry parameters

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