International safety notice
Urgent field safety notice for DuraDiagnost and DuraDiagnost Compact x-ray system, Philips Healthcare
Germany / BfArM · DEU · Jan 10, 2017
Key facts
| Title | Urgent field safety notice for DuraDiagnost and DuraDiagnost Compact x-ray system, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | DuraDiagnost and DuraDiagnost Compact x-ray system, Philips Healthcare |
| Manufacturer | Urgent field safety notice for DuraDiagnost and DuraDiagnost Compact x-ray system, Philips Healthcare |
| Models | 2.1.0, 712212, 2.0.0, 712210, 2.1.2, 2.0.1, 1.0.1, 1.0.2, 2.1.1, 1.0.0, PX4343RG, FCO71200154 and 2 more |
| Date | Jan 10, 2017 |
| 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