International safety notice
Information for Allura Xper FD10 and FD10/10, Philips
Germany / BfArM · DEU · Jul 7, 2008
Key facts
| Title | Information for Allura Xper FD10 and FD10/10, Philips |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Allura Xper FD10 and FD10/10, Philips |
| Manufacturer | Information for Allura Xper FD10 and FD10/10, Philips |
| Models | 2008-05-21, XDB087-080314, 2007-11-30, UXW-060003A2, FC072200111, 722001, 72200125, 1-125 |
| Date | Jul 7, 2008 |
| 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