Data / Medical devices / Electrocardiograph / Germany
FDA-registered makers of Electrocardiograph in Germany: 8 establishments
8 establishments in Germany are registered with the FDA to make Electrocardiograph (product code DPS). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Electrocardiograph
- Product code
- DPS
- Country
- Germany
Makers of Electrocardiograph in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Philips Medizin Systeme Boeblingen GmbH | BOEBLINGEN Baden-Wurttemberg, Germany | Complaint file establishment, Manufacturer, Specification developer | 5 | December 17, 2024 | 0 | 0 | 0 | api.fda.gov |
| Corscience GMBH & Co. KG | ERLANGEN Bavaria, Germany | Complaint file establishment, Specification developer | 1 | December 28, 2018 | 0 | 0 | 0 | api.fda.gov |
| eResearchTechnology GmbH | Estenfeld Bavaria, Germany | Complaint file establishment, Manufacturer | 1 | May 4, 2007 | 0 | 0 | 0 | api.fda.gov |
| Bernd Richter GMBH | Wipperfuerth North Rhine-Westphalia, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GWW | Gaertringen Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jaeger Medical GmbH | HOECHBERG Bavaria, Germany | Complaint file establishment, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pulsion Medical Systems Se | Aschheim, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Waltron GMBH | Wolnzach Bavaria, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.