International safety notice
Problem with Axiom Artis system VB11D or VB20B software from Siemens
Germany / BfArM · DEU · May 24, 2005
Key facts
| Title | Problem with Axiom Artis system VB11D or VB20B software from Siemens |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Problem with Axiom Artis system VB11D or VB20B software from Siemens |
| Manufacturer | Problem with Axiom Artis system VB11D or VB20B software from Siemens |
| Models | 18-8069, D-91301, D-91294, MO5ED•T, 12300, 0919111&9912, 09191, VB20B, 27-APRIL-2005 |
| Date | May 24, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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