Singapore HSA registration DE0507958
Diasorin LIAISON® Direct Renin
Device classification
- Device Class
- CLASS B IVD
- Medical Speciality Area
- Immunology
Registration information
- Registration Number
- DE0507958
- Registration Date
- March 30, 2023
- Retention Due Date
- March 29, 2026
Product description
The LIAISON® Direct Renin assay uses chemiluminescence immunoassay (CLIA) technology for the in vitro quantitative determination of renin in human EDTA-plasma specimens. Renin measurement is of help in the diagnosis and treatment of a number of hypertension types in humans. The test has to be performed on the LIAISON® Analyzer family.
Product Owner
- Short Name
- DiaSorin Italia S.p.A.
- Address
- Via Crescentino, snc, 13040 Saluggia (VC) Italy, ITALY
Registrant
- Address
- 100H PASIR PANJANG ROAD, OC@PASIR PANJANG, #07-01, SINGAPORE 118524
Importer
- Address
- 100H PASIR PANJANG ROAD, OC@PASIR PANJANG, #07-01, SINGAPORE 118524
Model information
- Model Name(s)
- LIAISON Direct Renin LIAISON Control Direct Renin
- Model Identifier(s)
- 310470 310471
About this record
Access comprehensive regulatory information for Diasorin LIAISON® Direct Renin in the Singapore medical device market through Pure Global AI's free database. This CLASS B IVD medical device is registered under HSA registration number DE0507958 and owned by DiaSorin Italia S.p.A.. The device was registered on March 30, 2023.
This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.
Free DatabasePowered by Pure Global AIHSA Official DataCLASS B IVD