International safety notice
Safety Notice for AXIOM Aristos FX Plus Systems, Siemens Healthcare
Germany / BfArM · DEU · Jan 16, 2012
Key facts
| Title | Safety Notice for AXIOM Aristos FX Plus Systems, Siemens Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | AXIOM Aristos FX Plus Systems, Siemens Healthcare |
| Manufacturer | Safety Notice for AXIOM Aristos FX Plus Systems, Siemens Healthcare |
| Models | 1-12-12, 10093864, 84-6060, 23691322, 12300, 91052, 84-9908, 2011-12-12 |
| Date | Jan 16, 2012 |
| 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