Pure Global

Fully automated clinical chemistry analyser - India CDSCO Medical Device Registration

Fully automated clinical chemistry analyser is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000132_48aa3fec75b8f161bf55e8ceed60e16b_0ea6b8c746bf2bba33f2b0d59ad9fd56. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class A
Fully automated clinical chemistry analyser
UID: MFG/IVD/2023/000132_48aa3fec75b8f161bf55e8ceed60e16b_0ea6b8c746bf2bba33f2b0d59ad9fd56

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.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing