International safety notice
Safety Notice concerning a corrective action of the Philips Invivo Expression MRI Patient Monitoring System, Philips Healthcare
Germany / BfArM · DEU · Jul 8, 2011
Key facts
| Title | Safety Notice concerning a corrective action of the Philips Invivo Expression MRI Patient Monitoring System, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Safety Notice concerning a corrective action of the Philips Invivo Expression MRI Patient Monitoring System, Philips Healthcare |
| Manufacturer | Safety Notice concerning a corrective action of the Philips Invivo Expression MRI Patient Monitoring System, Philips Healthcare |
| Models | US93600144, US00201003, US00200143, US00200294, US00200745, US00200558, US00201382, US00200170, US00200568, US00201451, US00200978, US00201225 and 278 more |
| Date | Jul 8, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching catalog numbers 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