International safety notice
Safety Notice for Allura Xper, Allura Integris, Multi Diagnost Eleva and Omni Diagnost Eleva X-ray systems, Philips
Germany / BfArM · DEU · Nov 10, 2010
Key facts
| Title | Safety Notice for Allura Xper, Allura Integris, Multi Diagnost Eleva and Omni Diagnost Eleva X-ray systems, Philips |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Allura Xper, Allura Integris, Multi Diagnost Eleva and Omni Diagnost Eleva X-ray systems, Philips |
| Manufacturer | Safety Notice for Allura Xper, Allura Integris, Multi Diagnost Eleva and Omni Diagnost Eleva X-ray systems, Philips |
| Models | FC070800115, 722006, 72242, 722004, 72246, 708034, UXWGÜ3A2, 722002, 708033, 708032, 2007-11-30, 722008 and 15 more |
| Date | Nov 10, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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