International safety notice
Important Safety Notice for AXIOM Artis, Artis zee or Artis Q systems, Siemens Healthcare
Germany / BfArM · DEU · Apr 16, 2014
Key facts
| Title | Important Safety Notice for AXIOM Artis, Artis zee or Artis Q systems, Siemens Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | AXIOM Artis, Artis zee or Artis Q systems, Siemens Healthcare |
| Manufacturer | Important Safety Notice for AXIOM Artis, Artis zee or Artis Q systems, Siemens Healthcare |
| Models | 91301, V13.06, 12300, 23691322, AX053, 2013-03-26 |
| Date | Apr 16, 2014 |
| 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