Typhoid Rapid Test Ki
- UID
- MFG/IVD/2020/000001_ee2bb694944499268457c5188a043ad7_d14bef988816d252e5645832587c8404
- Device class
- Class B
- License holder
- M/S. MEDSOURCE OZONE BIOMEDICALS PVT LTD
- Approving authority
- Haryana
- Product information
- Rapid immunochromatographic assay for qualitative detection and differentiation of IgG & IgM antibodies of Salmonella typhi and paratyphi in human serum/ plasma
Typhoid Rapid Test Ki is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000001_ee2bb694944499268457c5188a043ad7_d14bef988816d252e5645832587c8404. The license holder is M/S. MEDSOURCE OZONE BIOMEDICALS PVT LTD, and it is classified as Device Class Class B. The approving authority is Haryana.
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