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.
Brand Name
GP
License Holder
Vector Biotek Pvt LtdDevice Class
Approving Authority
CDSCO
Product Information
A device used to measures the volume of the antigen/antibody present in the components of body fluids.
Immunofluorescence Quantitative Analyzer
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