Siemens N Antiserum to Human Plasminogen - HSA Registration DE0017822
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.
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.