SD BIOLINE Syphilis Fast 3.0 - India CDSCO Medical Device Registration
SD BIOLINE Syphilis Fast 3.0 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000156_aede523f638edf6f14dbde8169e7bd0f_1313326c81f32cb742a9f4eaf3b54669. This device is marketed under the brand name SD BIOLINE Syphilis Fast 3.0. The license holder is Abbott Diagnostics Medical Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.
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Brand Name
SD BIOLINE Syphilis Fast 3.0
License Holder
Abbott Diagnostics Medical Private LimitedDevice Class
Approving Authority
CDSCO
Product Information
SD BIOLINE Syphilis Fast 3.0 test is a solid phase immunochromatographic assay for the qualitative detection of antibodies of all isotypes(SD BIOLINE Syphilis Fast 3.0) against Treponema pallidum (SD BIOLINE Syphilis Fast 3.0). This test is intended for professional use as an aid on the diagnosis of syphilis
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Dengue IgM Capture ELISA
Brand: SD BIOLINE Dengue IgG/IgM WB
BIOLINE Dengue NS1 Ag
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SD BIOLINE Tsutsugamushi
Brand: SD BIOLINE Dengue IgG/IgM WB
SD BIOLINE AFP
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SD BIOLINE Leptospira
Brand: SD BIOLINE Dengue IgG/IgM WB
BIOLINE HCV
Brand: SD BIOLINE Syphilis Fast 3.0
BIOLINE HCV
Brand: SD BIOLINE Syphilis Fast 3.0
SD BIOLINE Influenza Antigen
Brand: SD BIOLINE Influenza Antigen

