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One Step rapid test kit for detection of Syphilis Ab - India CDSCO Medical Device Registration

One Step rapid test kit for detection of Syphilis Ab is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000005_d70a7d2aa186225503bdc8d8bc225230_5f000c42621c12b9b08f7455884d15d0. This device is marketed under the brand name Standard Q HIV 1/2 Ab 4-line ,Ultra HIV 1/2 Ab 4-line. The license holder is SD Biosensor Healthcare Pvt. Ltd, and it is classified as Device Class Class D. The approving authority is Sub Zonal Baddi.

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CDSCO Registered
Class Class D
One Step rapid test kit for detection of Syphilis Ab
UID: MFG/MD/2018/000005_d70a7d2aa186225503bdc8d8bc225230_5f000c42621c12b9b08f7455884d15d0

Brand Name

Standard Q HIV 1/2 Ab 4-line ,Ultra HIV 1/2 Ab 4-line

Device Class

Class D

Approving Authority

Sub Zonal Baddi

Product Information

It is a rapid chromatographic immunoassay for the qualitative detection of anti-syphilis from human serum, plasma or whole blood. This test is for professional in vitro diagnostic use and intended as an aid to early diagnosis of syphilis infection

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DJ Fang

DJ Fang

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