SYPHILIS RAPID TEST KIT - India CDSCO Medical Device Registration

SYPHILIS RAPID TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000053_14b14de5d505206ab56c7774ae3964cf_98f24466866573db67259b1f576988b2. This device is marketed under the brand name HBsAg ELISA Kit, Labsystems Diagnostics . The license holder is Trivitron Healthcare Pvt. Ltd, and it is classified as Device Class Class D. The approving authority is Central Drug Standard Control Organisation, South Zone.

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CDSCO Registered

Class Class D

SYPHILIS RAPID TEST KIT

UID: MFG/IVD/2020/000053_14b14de5d505206ab56c7774ae3964cf_98f24466866573db67259b1f576988b2

Brand Name

HBsAg ELISA Kit, Labsystems Diagnostics

License Holder

Trivitron Healthcare Pvt. Ltd

Device Class

Class D

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

Biocard SYPHILIS Rapid test is an Immunochromatographic assay for the qualitative detection of antibodies (HBsAg ELISA Kit, Labsystems Diagnostics ) to Treponema pallidum in human serum, plasma and Whole Blood