Data / Medical devices / Full-Montage Standard Electroencephalograph / Germany
FDA-registered makers of Full-Montage Standard Electroencephalograph in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Full-Montage Standard Electroencephalograph (product code GWQ). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Full-Montage Standard Electroencephalograph
- Product code
- GWQ
- Country
- Germany
Makers of Full-Montage Standard Electroencephalograph in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bee Medic GMBH | Bamberg Bavaria, Germany | Manufacturer | 1 | December 30, 2020 | 0 | 0 | 0 | api.fda.gov |
| Eemagine Medical Imaging Solutions GMBH | Berlin, Germany | Manufacturer | 1 | September 12, 2005 | 0 | 0 | 0 | api.fda.gov |
| Inomed Medizintechnik GMBH | EMMENDINGEN Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nicolay GMBH | NAGOLD Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips Medizin Systeme Boeblingen GmbH | BOEBLINGEN Baden-Wurttemberg, Germany | Complaint file establishment, Manufacturer, Specification developer | 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.