Diagnostics Test for Syphilis Rapid Test
- UID
- MFG/IVD/2019/000026_c41621073e2937bb997e2a920c961551_762a7ef74f77f253c6c0e107f1234ab4
- Device class
- Class D
- License holder
- Nucleus Diagnosys LLP
- Approving authority
- Central Drug Standards Control Organization, Ahmedabad
- Product information
- Syphilis test reagents/kits is a medical device intended for the screening of Syphilis in blood/body fluids
Diagnostics Test for Syphilis Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000026_c41621073e2937bb997e2a920c961551_762a7ef74f77f253c6c0e107f1234ab4. The license holder is Nucleus Diagnosys LLP, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.
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