International safety notice
lmportant customer safety notice for AXIOM Artis FA, FC, dFA, dFC, dFCM, AXIOM Artis BA, BC, dBA, dBC, dBCM and AXIOM Artis MP, dMP Systems with SW version VB23N/P, Siemens Healthcare GmbH
Germany / BfArM · DEU · Oct 8, 2015
Key facts
| Title | lmportant customer safety notice for AXIOM Artis FA, FC, dFA, dFC, dFCM, AXIOM Artis BA, BC, dBA, dBC, dBCM and AXIOM Artis MP, dMP Systems with SW version VB23N/P, Siemens Healthcare GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | AXIOM Artis FA, FC, dFA, dFC, dFCM, AXIOM Artis BA, BC, dBA, dBC, dBCM and AXIOM Artis MP, dMP Systems with SW version VB23N/P, Siemens Healthcare GmbH |
| Manufacturer | lmportant customer safety notice for AXIOM Artis FA, FC, dFA, dFC, dFCM, AXIOM Artis BA, BC, dBA, dBC, dBCM and AXIOM Artis MP, dMP Systems with SW version VB23N/P, Siemens Healthcare GmbH |
| Models | 213821, AX050, 91301, VB23N, AX051, 64872105, 2015-09-01 |
| Date | Oct 8, 2015 |
| 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