LIAISON Light Check 12 - India CDSCO Medical Device Registration

LIAISON Light Check 12 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000089_776eb487166900ad7d571dc9570733c0_254d6f1913d495da855957b782001b6a. This device is marketed under the brand name LIAISON Light Check 12. 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.

Free Database

CDSCO Registered

Class Class A

LIAISON Light Check 12

UID: IMP/IVD/2019/000089_776eb487166900ad7d571dc9570733c0_254d6f1913d495da855957b782001b6a

Brand Name

LIAISON Light Check 12

License Holder

Diasorin Healthcare India Pvt. Ltd.

Device Class

Class A

Approving Authority

CDSCO

Product Information

Light Check reagent required to check the validity of starter reagents Starter 1 and 2 as well as the functioning of the measurement and pipetting units. A Light Check has to be carried out on the LIAISON® Analyzer either once daily prior to starting the first measurement series or each time a new lot of starter reagents is used. This control programme concomitantly checks the proper functioning of the instrument and of the starter reagents to avoid data loss due to instrument defects or inadvertently placed or expired starter reagents