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/2019/000113_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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Brand Name
LIAISON fPSA
License Holder
Diasorin Healthcare India Pvt. Ltd.Device Class
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
LIAISON® Analyzer
Brand: LIAISON® Analyzer
LIAISON® XS
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LIAISON® Q.S.E.T. Device Plus
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LIAISON fPSA Control
Brand: LIAISON fPSA
LIAISON PSA Control
Brand: LIAISON fPSA
LIAISON PSA
Brand: LIAISON fPSA
LIAISON® PSA
Brand: LIAISON® Tg II Gen Confirmatory
LIAISON IGF-1 Control
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LIAISON tTG IgA Control
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LIAISON XL Starter Kit
Brand: LIAISON Light Check 12