International safety notice
Corrective action for the OEC 9800, FlexiView 8800, OEC MiniView 6800 and OEC UroView 2800 systems, GE Healthcare
Germany / BfArM · DEU · Oct 29, 2014
Key facts
| Title | Corrective action for the OEC 9800, FlexiView 8800, OEC MiniView 6800 and OEC UroView 2800 systems, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the OEC 9800, FlexiView 8800, OEC MiniView 6800 and OEC UroView 2800 systems, GE Healthcare |
| Manufacturer | Corrective action for the OEC 9800, FlexiView 8800, OEC MiniView 6800 and OEC UroView 2800 systems, GE Healthcare |
| Models | 8S-2554, 82-2454, 82-2535, 82-7103-MH, 82-2655, 86-0931, 82-2751, 8S-2675, 82-3226, 89-3531, 89-2690, 82-1731 and 335 more |
| Date | Oct 29, 2014 |
| 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