Data / Medical devices / Injector, Contrast Medium, Automatic / Germany
FDA-registered makers of Injector, Contrast Medium, Automatic in Germany: 6 establishments
6 establishments in Germany are registered with the FDA to make Injector, Contrast Medium, Automatic (product code IZQ). 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
- Injector, Contrast Medium, Automatic
- Product code
- IZQ
- Country
- Germany
Makers of Injector, Contrast Medium, Automatic in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ulrich GMBH & Co. KG | ULM Baden-Wurttemberg, Germany | Manufacturer | 7 | November 18, 2025 | 0 | 0 | 0 | api.fda.gov |
| Ulrich GMBH & Co. KG | Dornstadt Baden-Wurttemberg, Germany | Manufacturer | 2 | November 18, 2025 | 0 | 0 | 0 | api.fda.gov |
| Bytec Medizintechnik GMBH | Eschweiler North Rhine-Westphalia, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gerresheimer Regensburg GmbH | Wackersdorf Bavaria, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Infumed GMBH | Friedeburg Lower Saxony, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lre Medical GMBH | NOERDLINGEN Bavaria, Germany | Contract 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.