International safety notice
Safety Notice for iCentral and iCentral Clients v5.0.2, GE Healthcare Finland Oy
Germany / BfArM · DEU · Jun 8, 2010
Key facts
| Title | Safety Notice for iCentral and iCentral Clients v5.0.2, GE Healthcare Finland Oy |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | iCentral and iCentral Clients v5.0.2, GE Healthcare Finland Oy |
| Manufacturer | Safety Notice for iCentral and iCentral Clients v5.0.2, GE Healthcare Finland Oy |
| Models | RP2130, XW4400, 53226, FL-00031, 79111, V5.0.2, XW4600, FM136052, V5.O.2 |
| Date | Jun 8, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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