CDSCO UID IMP/IVD/2019/000089_776eb487166900ad7d571dc9570733c0_254d6f1913d495da855957b782001b6aLIAISON Light Check 12
- UID
- IMP/IVD/2019/000089_776eb487166900ad7d571dc9570733c0_254d6f1913d495da855957b782001b6a
- Device class
- Class A
- Brand name
- LIAISON Light Check 12
- License holder
- Diasorin Healthcare India Pvt. Ltd.
- 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
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.
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