International safety notice
Urgent Safety Notice for the CDAS upgraded Intera MR systems equipped with the Basic Triggering Unit, Philips Healthcare
Germany / BfArM · DEU · Dec 30, 2014
Key facts
| Title | Urgent Safety Notice for the CDAS upgraded Intera MR systems equipped with the Basic Triggering Unit, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the CDAS upgraded Intera MR systems equipped with the Basic Triggering Unit, Philips Healthcare |
| Manufacturer | Urgent Safety Notice for the CDAS upgraded Intera MR systems equipped with the Basic Triggering Unit, Philips Healthcare |
| Models | 453564099151, 452213224623, 00425, 452213224543, 452215033673, FSN78100425 |
| Date | Dec 30, 2014 |
| 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