COVID 19 IGG/IGM RAPID TEST - India CDSCO Medical Device Registration
COVID 19 IGG/IGM RAPID TEST is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000033_b34d35356fd8d8b6c43bdc07427d66a4_0a2bb6c84c13b18e2ebd38c1974624f8. The license holder is M/S. MEDSOURCE OZONE BIOMEDICALS PVT LTD, and it is classified as Device Class Class C. The approving authority is Sub Zonal Baddi.
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
M/S. MEDSOURCE OZONE BIOMEDICALS PVT LTDDevice Class
Approving Authority
Sub Zonal Baddi
Product Information
COVID 19 IgG/IgM Test kit is a rapid immunochromatography assay used for qualitative determination of IgG and IgM antibodies to 2019 novel coronavirus in human serum, plasma, or whole blood.
