Syphilis Ab Rapid Test - India CDSCO Medical Device Registration
Syphilis Ab Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000139_599b32e873699a913259abc373b9d3fd_fb9ea1776e4351aa1e5b1a9ddd742039. The license holder is LABGENE BIO-TECH PRIVATE LIMITED, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.
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License Holder
LABGENE BIO-TECH PRIVATE LIMITEDDevice Class
Approving Authority
Central Drug Standards Control Organization, Ahmedabad
Product Information
The Syphilis Ab Rapid test kit is a rapid immunochromatography assay for the qualitative detection of antibodies against Treponema pallidum in human whole blood, serum or plasma samples
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