International safety notice
Corrective action concerning the Integris and Allura Xper X-Ray Systems from Philips
Germany / BfArM · DEU · Jan 30, 2007
Key facts
| Title | Corrective action concerning the Integris and Allura Xper X-Ray Systems from Philips |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corrective action concerning the Integris and Allura Xper X-Ray Systems from Philips |
| Manufacturer | Corrective action concerning the Integris and Allura Xper X-Ray Systems from Philips |
| Models | 02-112006, 02-11-2006, FC0072200091, 62205, 14-07-2006, XDB087-060657, 17060498, 2006-11-10 |
| Date | Jan 30, 2007 |
| 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