LIAISON® fPSA - India CDSCO Medical Device Registration

LIAISON® fPSA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000089_86ba3c78fc0796f54a9187319497b5c0_0eb377493814e1fccf6195878e92b4a9. This device is marketed under the brand name LIAISON® Tg II Gen Confirmatory. The license holder is Diasorin Healthcare India Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered

Class Class C

LIAISON® fPSA

UID: IMP/IVD/2019/000089_86ba3c78fc0796f54a9187319497b5c0_0eb377493814e1fccf6195878e92b4a9

Brand Name

LIAISON® Tg II Gen Confirmatory

License Holder

Diasorin Healthcare India Pvt. Ltd.

Device Class

Class C

Approving Authority

CDSCO

Product Information

In vitro assay for the quantitative determination of free human prostate-specific antigen (LIAISON® Tg II Gen Confirmatory) in human serum and plasma (LIAISON® Tg II Gen Confirmatory). The test has to be performed on the LIAISON® Analyzer family

Class C

Brand: LIAISON® EASY System Liquid

Class B