LIAISON® Q.S.E.T. Device Plus - India CDSCO Medical Device Registration
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.
This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Brand Name
LIAISON® Q.S.E.T. Device Plus
License Holder
Diasorin Healthcare India Pvt. Ltd.Device Class
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.
LIAISON® Analyzer
Brand: LIAISON® Analyzer
LIAISON® XS
Brand: LIAISON® XS
LIAISON fPSA Control
Brand: LIAISON fPSA
LIAISON PSA Control
Brand: LIAISON fPSA
LIAISON fPSA
Brand: LIAISON fPSA
LIAISON PSA
Brand: LIAISON fPSA
LIAISON® PSA
Brand: LIAISON® Tg II Gen Confirmatory
LIAISON IGF-1 Control
Brand: LIAISON® EASY System Liquid
LIAISON tTG IgA Control
Brand: LIAISON® EASY System Liquid
LIAISON XL Starter Kit
Brand: LIAISON Light Check 12