International safety notice
Safety Notice for MultiDiagnost Eleva, UroDiagnost Eleva and OmniDiagnost Eleva Systems, Philips Healthcare
Germany / BfArM · DEU · Mar 27, 2009
Key facts
| Title | Safety Notice for MultiDiagnost Eleva, UroDiagnost Eleva and OmniDiagnost Eleva Systems, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | MultiDiagnost Eleva, UroDiagnost Eleva and OmniDiagnost Eleva Systems, Philips Healthcare |
| Manufacturer | Safety Notice for MultiDiagnost Eleva, UroDiagnost Eleva and OmniDiagnost Eleva Systems, Philips Healthcare |
| Models | FSN-70800070, 2007-12-18, UXW-060003A2, FC070800070, XDB090005 |
| Date | Mar 27, 2009 |
| 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