International safety notice
Safety Notice concerning corrective actions for X-ray system VIDIX U (Universal Type), Tetenal
Germany / BfArM · DEU · Aug 31, 2011
Key facts
| Title | Safety Notice concerning corrective actions for X-ray system VIDIX U (Universal Type), Tetenal |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | X-ray system VIDIX U (Universal Type), Tetenal |
| Manufacturer | Safety Notice concerning corrective actions for X-ray system VIDIX U (Universal Type), Tetenal |
| Models | 134374724, D-22844, D-22841, 91224, 44522, PBNKDEFF200, 31-35, DE39370106001031551850 |
| Date | Aug 31, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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