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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 MFG/IVD/2023/000132_c2306a1f799ce8c8daa15a0aac630bfc_ed1e420312a4c8fc90132e5e6f9a6ffd. This device is marketed under the brand name DiaSys. The license holder is DiaSys Diagnostics India Private Limited, and it is classified as Device Class Class A. The approving authority is Kokan Division.

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: MFG/IVD/2023/000132_c2306a1f799ce8c8daa15a0aac630bfc_ed1e420312a4c8fc90132e5e6f9a6ffd

Brand Name

DiaSys

Device Class

Class A

Approving Authority

Kokan Division

Product Information

The product is a fully automated clinical chemistry analyzer for quantitative analysis of chemical components in human samples (DiaSys), which can assist in the diagnosis of normal people and patients with related diseases. The product has no independent measuring function and uses the supporting biochemical reagent kit manufactured by DiaSys to finish testing. The detectable indicators include: liver function, renal function, ion-metabolization, blood sugar, blood fat, myocardium enzymogram, immunity and other items

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