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CDSCO UID IMP/IVD/2019/000113_1fde04a38f8f29c96e9fb07e25fe1f24_4b4e68072f0d4a4935292b4a8b9f1857

LIAISON PSA

Diasorin Healthcare India Pvt. Ltd.·Device Class Class C·India CDSCO·Brand: LIAISON fPSA
Registration details
UID
IMP/IVD/2019/000113_1fde04a38f8f29c96e9fb07e25fe1f24_4b4e68072f0d4a4935292b4a8b9f1857
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 human prostate-specific antigen (LIAISON fPSA) in human serum and plasma (LIAISON fPSA) during the follow-up of patients with carcinoma of the prostate. The test has to be performed on the LIAISON® Analyzer family.
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About this record

LIAISON PSA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000113_1fde04a38f8f29c96e9fb07e25fe1f24_4b4e68072f0d4a4935292b4a8b9f1857. 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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