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CDSCO UID IMP/IVD/2022/000360_c7e21e1429ed76d72f9b7878e6bf5410_3a191d6c336652a536bc4c15f0425b17

LIAISON® Q.S.E.T. Device Plus

Diasorin Healthcare India Pvt. Ltd.·Device Class Class A·India CDSCO·Brand: LIAISON® Q.S.E.T. Device Plus
Registration details
UID
IMP/IVD/2022/000360_c7e21e1429ed76d72f9b7878e6bf5410_3a191d6c336652a536bc4c15f0425b17
Device class
Class A
Brand name
LIAISON® Q.S.E.T. Device Plus
License holder
Diasorin Healthcare India Pvt. Ltd.
Approving authority
CDSCO
Product information
The LIAISON® Q.S.E.T. Device Plus (LIAISON® Q.S.E.T. Device Plus) is intended for use in the preparation of human stool specimens for testing in designated stool assays. The device is intended for in vitro diagnostic use in a professional laboratory setting on the automated LIAISON® Analyzer family.
Other products from Diasorin Healthcare India Pvt. Ltd.
Products from the same license holder (10 products)
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LIAISON fPSA
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LIAISON PSA
Brand: LIAISON fPSA
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LIAISON® PSA
Brand: LIAISON® Tg II Gen Confirmatory
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LIAISON IGF-1 Control
Brand: LIAISON® EASY System Liquid
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LIAISON tTG IgA Control
Brand: LIAISON® EASY System Liquid
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LIAISON XL Starter Kit
Brand: LIAISON Light Check 12
Class A
About this record

LIAISON® Q.S.E.T. Device Plus is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000360_c7e21e1429ed76d72f9b7878e6bf5410_3a191d6c336652a536bc4c15f0425b17. This device is marketed under the brand name LIAISON® Q.S.E.T. Device Plus. The license holder is Diasorin Healthcare India Pvt. Ltd., and it is classified as Device Class Class A. The approving authority is CDSCO.

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