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Immunofluorescence Quantitative Analyzer - India CDSCO Medical Device Registration

Immunofluorescence Quantitative Analyzer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000153_ced6aed3d9eee968c95db30075aef2e6_67031b259b38bc4a2c4f1e23d972906a. The license holder is Cipla Limited, 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
Immunofluorescence Quantitative Analyzer
UID: IMP/IVD/2022/000153_ced6aed3d9eee968c95db30075aef2e6_67031b259b38bc4a2c4f1e23d972906a

License Holder

Cipla Limited

Device Class

Class A

Approving Authority

CDSCO

Product Information

Getein1180 Immunofluorescence Quantitative Analyzer ##PLACEHOLDER_0## is an analyzer for processing and analysis of Getein test kits including markers for cardiovascular diseases, renal diseases, inflammation, fertility, diabetes mellitus, bone metabolism, tumor and thyroid.and Acute Coronary Syndrome ##PLACEHOLDER_0##.

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