International safety notice
Safety Notice for Philips Precess MRI Patient Monitoring System
Germany / BfArM · DEU · Nov 7, 2011
Key facts
| Title | Safety Notice for Philips Precess MRI Patient Monitoring System |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Philips Precess MRI Patient Monitoring System |
| Manufacturer | Safety Notice for Philips Precess MRI Patient Monitoring System |
| Models | 00322, 0000A30212, 00220, 0000A30449, 20304, 00196, 0000A30712, 0000A30656, 0000A30797, 0000A30440, 0000A30784, 0000A30637 and 555 more |
| Date | Nov 7, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1,000+ Matching device models in FDA data
- 100–999 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