Pure Global

LIAISON fPSA Control - India CDSCO Medical Device Registration

LIAISON fPSA Control is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000113_7a831c6a288b839ebd6243954a3c4d30_575fc14f7b68f028d8d10acbc0b46f2e. 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.

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
Powered by Pure Global AI
CDSCO Registered
Class Class C
LIAISON fPSA Control
UID: IMP/IVD/2019/000113_7a831c6a288b839ebd6243954a3c4d30_575fc14f7b68f028d8d10acbc0b46f2e

Brand Name

LIAISON fPSA

Device Class

Class C

Approving Authority

CDSCO

Product Information

The LIAISON® fPSA controls (LIAISON fPSA) are to be used in LIAISON® fPSA chemiluminescent immunoassays (LIAISON fPSA) as a means of checking reliability of assay runs. The performance characteristics of LIAISON® Control fPSA have not been established for any other assays or instrument platforms different from LIAISON® and LIAISON® XL

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing