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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/2019/000410_ced6aed3d9eee968c95db30075aef2e6_9830e601afd5f9884f22ebc9e9b15fe8. This device is marketed under the brand name GP. The license holder is Vector Biotek 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/2019/000410_ced6aed3d9eee968c95db30075aef2e6_9830e601afd5f9884f22ebc9e9b15fe8

Brand Name

GP

License Holder

Vector Biotek Pvt Ltd

Device Class

Class A

Approving Authority

CDSCO

Product Information

A device used to measures the volume of the antigen/antibody present in the components of body fluids.

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