International safety notice
Urgent Field Safety Notice for syngo Imaging, syngo.plaza, syngo Dynamics, syngo Imaging XS, MagicLink A, syngo Workflow MLR (44087), syngo Workflow SLR (44087), syngo.via (57812), syngo.via ProtoNeo(57812) by Siemens AG, Medical Solutions, SYNGO, Henkestr. 127, DE-91052 Erlangen, Germany
Germany / BfArM · DEU · Jun 23, 2017
Key facts
| Title | Urgent Field Safety Notice for syngo Imaging, syngo.plaza, syngo Dynamics, syngo Imaging XS, MagicLink A, syngo Workflow MLR (44087), syngo Workflow SLR (44087), syngo.via (57812), syngo.via ProtoNeo(57812) by Siemens AG, Medical Solutions, SYNGO, Henkestr. 127, DE-91052 Erlangen, Germany |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | syngo Imaging, syngo.plaza, syngo Dynamics, syngo Imaging XS, MagicLink A, syngo Workflow MLR (44087), syngo Workflow SLR (44087), syngo.via (57812), syngo.via ProtoNeo(57812) |
| Manufacturer | Siemens AG, Medical Solutions, SYNGO, Henkestr. 127, DE-91052 Erlangen, Germany |
| Models | 139FTCP, V1306, 7-010.ASPXL, 64872105, I000W, SYNG0A, 17-010, 213821, 2017105, 91052, VA50B_0207, VF50A |
| Date | Jun 23, 2017 |
| 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