International safety notice
Corrective action for the IntelliVue MX40 patient monitor with software revisions B.00 and B.01, Philips Healthcare
Germany / BfArM · DEU · Jun 24, 2014
Key facts
| Title | Corrective action for the IntelliVue MX40 patient monitor with software revisions B.00 and B.01, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the IntelliVue MX40 patient monitor with software revisions B.00 and B.01, Philips Healthcare |
| Manufacturer | Corrective action for the IntelliVue MX40 patient monitor with software revisions B.00 and B.01, Philips Healthcare |
| Models | 86201560A, MX40”, 865350, B.00.X, 865352, 865351, B.01.X |
| Date | Jun 24, 2014 |
| 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