International safety notice
Urgent Field Safety Notice for Philips Hemodynamic Application R1.0 by Philips Medical Systems Nederland B.V.
Germany / BfArM · DEU · Jan 30, 2019
Key facts
| Title | Urgent Field Safety Notice for Philips Hemodynamic Application R1.0 by Philips Medical Systems Nederland B.V. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Philips Hemodynamic Application R1.0 |
| Manufacturer | Philips Medical Systems Nederland B.V. |
| Models | 722463, 1.0.1 |
| Date | Jan 30, 2019 |
| 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