HSA · registration DE0017822Siemens N Antiserum to Human Plasminogen
- Registration number
- DE0017822
- Model name
- N Antiserum to Human Plasminogen; N Protein Standard PY; N Reaction Buffer; N Diluent; N Supplementary Reagent/Precipitation; N/T Protein Control PY
- Model identifier
- OSCB09; OUID13; OUMS61; OUMT05; OUMU15; OWSY13
- Registration date
- January 26, 2016
- Source update date
- October 01, 2024
- Risk class
- Class B
- Product owner
- Siemens Healthcare Diagnostics Products GmbH
- Registrant / registration holder
- SIEMENS HEALTHCARE PTE. LTD.
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 address
- Emil-von-Behring-Str. 76, 35041 Marburg, Germany
- Registrant address
- 60 MACPHERSON ROAD, THE SIEMENS CENTRE, Singapore 348615
This page mirrors one row from HSA’s official registered-medical-device workbook. Product owner and registrant are separate published roles; neither is relabeled as the manufacturer. The official NOT_GENERATED value is retained when HSA does not publish a registration number, and the device name remains part of the stable record identity.