International safety notice
Advisory Notice for O-ARM® Intraoperative Imaging Systems, Medtronic
Germany / BfArM · DEU · Dec 21, 2007
Key facts
| Title | Advisory Notice for O-ARM® Intraoperative Imaging Systems, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | O-ARM® Intraoperative Imaging Systems, Medtronic |
| Manufacturer | Advisory Notice for O-ARM® Intraoperative Imaging Systems, Medtronic |
| Models | 9732461 |
| Date | Dec 21, 2007 |
| 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