International safety notice
Safety Notice for the Footswitch of the Allura FD10, FD20, CV20 systems and the Allura field extension series, Philips
Germany / BfArM · DEU · Jan 6, 2011
Key facts
| Title | Safety Notice for the Footswitch of the Allura FD10, FD20, CV20 systems and the Allura field extension series, Philips |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Footswitch of the Allura FD10, FD20, CV20 systems and the Allura field extension series, Philips |
| Manufacturer | Safety Notice for the Footswitch of the Allura FD10, FD20, CV20 systems and the Allura field extension series, Philips |
| Models | 722123, 722012, REPTOD1Æ00N, 72200189, 2007-12, UXW-060003A2, ALLURACV20, UXW-$OD03A2, 2007-12-18, 452270000141, 722010, XCR603-100401 and 3 more |
| Date | Jan 6, 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