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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_9e35fa2c6ab7b0bdda0f1e09f8fe578b. 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_9e35fa2c6ab7b0bdda0f1e09f8fe578b

Brand Name

HumaCLIA 150

Device Class

Class A

Approving Authority

CDSCO

Product Information

The HumaStar 300SR is an automatic random-access clinical chemistry analyzer specially designed and developed to perform clinical chemistry tests for in vitro diagnostic use (HumaCLIA 150 ). HumaStar 300SR is a system analyzer which is used with Human System Reagents

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