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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/2020/001031_c9e9a0fd6f8666e6a514b3cc7866d44e_279f290c25de7b969110383efbe1bc65. This device is marketed under the brand name Getein 1100 Immunofluorescence Quantitative analyzer. The license holder is M/s. Peerless Biotech 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
Immunofluorescence Quantitative analyzer
UID: IMP/IVD/2020/001031_c9e9a0fd6f8666e6a514b3cc7866d44e_279f290c25de7b969110383efbe1bc65

Brand Name

Getein 1100 Immunofluorescence Quantitative analyzer

Device Class

Class A

Approving Authority

CDSCO

Product Information

Getein1100 Immunofluorescence Quantitative Analyzer (Getein 1100 Immunofluorescence Quantitative analyzer) is an analyzer for processing Getein test kits and analysis of markers for cardiovascular diseases, renal diseases, inflammation, fertility, diabetes mellitus, bone metabolism, tumor and thyroid. This manual contains instructions for the use of Getein1100 and general instructions for testing specimens and quality control materials.

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