International safety notice
Urgent Safety Notice for Philips M3002 IntelliVue X2 and M8102A IntelliVue MP2, Philips Healthcare
Germany / BfArM · DEU · Oct 25, 2010
Key facts
| Title | Urgent Safety Notice for Philips M3002 IntelliVue X2 and M8102A IntelliVue MP2, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Philips M3002 IntelliVue X2 and M8102A IntelliVue MP2, Philips Healthcare |
| Manufacturer | Urgent Safety Notice for Philips M3002 IntelliVue X2 and M8102A IntelliVue MP2, Philips Healthcare |
| Models | DE83629383, DE95008299, FSN86201157, DE95052110, M8102A, X2AND, M3002A, DE83604981, M3002 |
| Date | Oct 25, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 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