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Fully Automated Clinical Chemistry Analyzer - India CDSCO Medical Device Registration

Fully Automated Clinical Chemistry Analyzer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000806_c2306a1f799ce8c8daa15a0aac630bfc_f38b268b1b0412cf5256ca6f1c34a956. This device is marketed under the brand name Nanolab 500 Fully Automated Clinical Chemistry Analyzer. The license holder is Trivitron Healthcare 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
Fully Automated Clinical Chemistry Analyzer
UID: IMP/IVD/2020/000806_c2306a1f799ce8c8daa15a0aac630bfc_f38b268b1b0412cf5256ca6f1c34a956

Brand Name

Nanolab 500 Fully Automated Clinical Chemistry Analyzer

Device Class

Class A

Approving Authority

CDSCO

Product Information

The system is a reliable in vitro diagnostic clinical chemistry analyzer for automatic testing of routine clinical chemistry tests and electrolytes. With a throughput of up to 300 photometric tests/hour.

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