Getein 1100 Immunofluorescence Quantitative Analyzer - India CDSCO Medical Device Registration
Getein 1100 Immunofluorescence Quantitative Analyzer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000403_ac18437d31286d73e7c56b6d7d36310f_72b54f8c217eaccf4242e8362be204f7. This device is marketed under the brand name GP. The license holder is M/s. Reckon Diagnostics Pvt. Ltd., and it is classified as Device Class Class A. The approving authority is CDSCO.
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Brand Name
GP
License Holder
M/s. Reckon Diagnostics Pvt. Ltd.Device Class
Approving Authority
CDSCO
Product Information
Getein1100 Immunofluorescence Quantitative Analyzer (GP) 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.
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