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CDSCO UID IMP/IVD/2019/000113_43f820ee9024b6f081e8d9bd085d3bb9_9756f8ca509b40695486b4b057d77831

LIAISON fPSA

Diasorin Healthcare India Pvt. Ltd.·Device Class Class C·India CDSCO·Brand: LIAISON fPSA
Registration details
UID
IMP/IVD/2019/000113_43f820ee9024b6f081e8d9bd085d3bb9_9756f8ca509b40695486b4b057d77831
Device class
Class C
Brand name
LIAISON fPSA
License holder
Diasorin Healthcare India Pvt. Ltd.
Approving authority
CDSCO
Product information
In vitro assay for the quantitative determination of free human prostate-specific antigen (LIAISON fPSA) in human serum and plasma (LIAISON fPSA). The test has to be performed on the LIAISON® Analyzer family
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About this record

LIAISON fPSA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000113_43f820ee9024b6f081e8d9bd085d3bb9_9756f8ca509b40695486b4b057d77831. This device is marketed under the brand name LIAISON fPSA. 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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