HBsAg Rapid Test - India CDSCO Medical Device Registration
HBsAg Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000016_d48047f9578cff055c32f1e8aca0818e_1533f58d9bebca88512e1e4e0fec09d9. The license holder is Genuine Biosystem Private Limited, and it is classified as Device Class Class D. The approving authority is Central Drug Standard Control Organisation, South Zone.
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.
License Holder
Genuine Biosystem Private LimitedDevice Class
Approving Authority
Central Drug Standard Control Organisation, South Zone
Product Information
A HBsAg Rapid Test is a medical device, intended for the detection of HBsAg in blood/body fluids
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