International safety notice
Corrective actions concerning the OEC UroView 2800 Systems from GE Healthcare
Germany / BfArM · DEU · Apr 5, 2007
Key facts
| Title | Corrective actions concerning the OEC UroView 2800 Systems from GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corrective actions concerning the OEC UroView 2800 Systems from GE Healthcare |
| Manufacturer | Corrective actions concerning the OEC UroView 2800 Systems from GE Healthcare |
| Models | 84116, UROVIEW9 |
| Date | Apr 5, 2007 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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