Syphilis Rapid Kit - India CDSCO Medical Device Registration
Syphilis Rapid Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000045_0855c7cb1b29c96c3191b7d841796360_04fb3aca6672bd23027d0c1a6bcf028b. The license holder is Promea Therapeutics Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO, Zonal office, Hyderabad.
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License Holder
Promea Therapeutics Private LimitedDevice Class
Approving Authority
CDSCO, Zonal office, Hyderabad
Product Information
A syphilis rapid kit is a rapid chromatographic immunoassay for the qualitative detection of antibodies ##PLACEHOLDER_0## to Treponema Pallidum ##PLACEHOLDER_0## in serum/plasma to aid in the diagnosis of Syphilis
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