International safety notice
Corrective action for the DuraDiagnost X-ray system, Philips Healthcare
Germany / BfArM · DEU · Jun 30, 2014
Key facts
| Title | Corrective action for the DuraDiagnost X-ray system, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the DuraDiagnost X-ray system, Philips Healthcare |
| Manufacturer | Corrective action for the DuraDiagnost X-ray system, Philips Healthcare |
| Models | SN130007, SN130004, SN120001, SN130023, SN130016, MAY29, SN130001, SN120002, SN130002, SN130012, SN120003, SN130010 and 16 more |
| Date | Jun 30, 2014 |
| 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