Singapore HSA registration DE0017822
Siemens N Antiserum to Human Plasminogen
Device classification
- Device Class
- CLASS B IVD
- Medical Speciality Area
- Immunology
Registration information
- Registration Number
- DE0017822
- Registration Date
- January 26, 2016
- Change Notification Approval Date
- October 01, 2024
- Retention Due Date
- January 25, 2026
Product description
N Antiserum to Human Plasminogen is an in vitro diagnostic reagent for the quantitative determination of plasminogen concentration as aid to diagnosis and monitoring of congenital or acquired plasminogen deficiencies in patients at risk for or suspected to have disorders of the fibrinolysis system in human sodium citrated plasma by means of automated Siemens Healthineers immuno-nephelometry systems. N Antiserum to Human Plasminogen uses a calibration against an internal protein reference preparation.
Product Owner
- Short Name
- Siemens Healthcare Diagnostics Products GmbH
- Address
- Emil-von-Behring-Str. 76, 35041 Marburg, GERMANY
Registrant
- Address
- 60 MACPHERSON ROAD, THE SIEMENS CENTRE, SINGAPORE 348615
Importer
- Address
- 60 MACPHERSON ROAD, THE SIEMENS CENTRE, SINGAPORE 348615
Model information
- Model Name(s)
- BN ProSpec System AP Update 3.0 CD Kit OUS N Antiserum to Human Plasminogen N Protein Standard PY N Reaction Buffer N Reaction Buffer N Diluent N Supplementary Reagent/Precipitation BN II System BN ProSpec System Atellica NEPH 630 System N/T Protein Control PY
- Model Identifier(s)
- 10987487 OSCB09 OUID13 OUMS61 OUMS65 OUMT05 OUMU15 OVIA11 OVLI01 OVLI02 (11239861) OWSY13
About this record
Access comprehensive regulatory information for Siemens N Antiserum to Human Plasminogen 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 DE0017822 and owned by Siemens Healthcare Diagnostics Products GmbH. The device was registered on January 26, 2016.
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