Data / Medical devices / Calculator/Data Processing Module, For Clinical Use / Germany
FDA-registered makers of Calculator/Data Processing Module, For Clinical Use in Germany: 10 establishments
10 establishments in Germany are registered with the FDA to make Calculator/Data Processing Module, For Clinical Use (product code JQP). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Calculator/Data Processing Module, For Clinical Use
- Product code
- JQP
- Country
- Germany
Makers of Calculator/Data Processing Module, For Clinical Use in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| AESKU.DIAGNOSTICS GmbH&Co.KG | WENDELSHEIM Rhineland-Palatinate, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Abbott Automation Solutions GmbH | Hamburg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beckman Coulter Biomedical GmbH | Baierbrunn Bavaria, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beckman Coulter Biomedical GmbH | Munchen Bavaria, Germany | Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Ekf Diagnostic GMBH | BARLEBEN/MADGEBURG Saxony-Anhalt, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips Medizin Systeme Boeblingen GmbH | BOEBLINGEN Baden-Wurttemberg, Germany | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Roche Diagnostics GMBH | MANNHEIM Baden-Wurttemberg, Germany | Exporter to the US, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Roche Diabetes Care GmbH | Mannheim Baden-Wurttemberg, Germany | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Roche Diagnostics Automation Solutions GmbH | Ludwigsburg Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthcare GmbH | Berlin, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.