Siemens Healthcare Diagnostic Products GmbH
GermanyFDA applicant, unverified
- Devices
- 5
Catalogue
INNOVANCE® D-Dimer 2.0 (SMN 10873803) Ref K253985
Regimes: 510(k) Registry: 510(k)INNOVANCE Antithrombin Ref K242952
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Automated Blood Coagulation Analyzer CS-2500 Ref K172286
Regimes: 510(k) Registry: 510(k)CardioPhase® hsCRP Ref K232624
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Siemens Healthcare Diagnostic Products GmbH have in the registry?
The registry currently lists 5 devices for Siemens Healthcare Diagnostic Products GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Siemens Healthcare Diagnostic Products GmbH's devices?
Among its 5 most recently registered devices, Siemens Healthcare Diagnostic Products GmbH has devices listed in FDA 510(k) (5 devices).
What risk classes do Siemens Healthcare Diagnostic Products GmbH's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Siemens Healthcare Diagnostic Products GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Siemens Healthcare Diagnostic Products GmbH in the registry?
The most recently registered devices listed for Siemens Healthcare Diagnostic Products GmbH include INNOVANCE® D-Dimer 2.0 (SMN 10873803), INNOVANCE Antithrombin, Sysmex Automated Blood Coagulation Analyzer CS-5100 and Automated Blood Coagulation Analyzer CS-2500.