International safety notice
Safety Notice for mobile X-Ray systems (Optima XR220amx, Optima XR200amx with Digital Upgrade), GE Healthcare
Germany / BfArM · DEU · Dec 30, 2013
Key facts
| Title | Safety Notice for mobile X-Ray systems (Optima XR220amx, Optima XR200amx with Digital Upgrade), GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | mobile X-Ray systems (Optima XR220amx, Optima XR200amx with Digital Upgrade), GE Healthcare |
| Manufacturer | Safety Notice for mobile X-Ray systems (Optima XR220amx, Optima XR200amx with Digital Upgrade), GE Healthcare |
| Models | 5421698, FMI10883_FSN_ENGLISH, 10883, 53226, XR220AMX, 5555000-6, 5555000-5, XR200AMX |
| Date | Dec 30, 2013 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1