International safety notice
Safety Notice for the Philips Allura Xper systems and Allura CV20, Philips
Germany / BfArM · DEU · Aug 30, 2011
Key facts
| Title | Safety Notice for the Philips Allura Xper systems and Allura CV20, Philips |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Philips Allura Xper systems and Allura CV20, Philips |
| Manufacturer | Safety Notice for the Philips Allura Xper systems and Allura CV20, Philips |
| Models | 722003, FC072200200, 6.5.2, 2007-12-18, 722006, XCR603-110071, UXW-060003A2, FD20120, 722014, 722019, 7.0.X, 722015 and 6 more |
| Date | Aug 30, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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