Getein 1600 Immunofluorescence Quantitative Analyzer
- UID
- IMP/IVD/2019/000403_3603fa7d864077e019ab6a516c95bc9f_ed6eb343cae6426498475818de17f5d6
- Device class
- Class A
- Brand name
- GP
- License holder
- M/s. Reckon Diagnostics Pvt. Ltd.
- Approving authority
- CDSCO
- Product information
- In conjunction with dedicated test kits for Immunofluorescence, the instrument automates the detection and quantification of markers for cardiovascular disease, renal diseases, inflammation, fertility, diabetes mellitus, bone metabolism, tumor and thyroid in a biological sample
Getein 1600 Immunofluorescence Quantitative Analyzer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000403_3603fa7d864077e019ab6a516c95bc9f_ed6eb343cae6426498475818de17f5d6. 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.
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.