International safety notice
Problem of undesirable behavior in specific reporting workflow in syngo Dynamics 9.0, Siemens Healthcare
Germany / BfArM · DEU · Jun 15, 2011
Key facts
| Title | Problem of undesirable behavior in specific reporting workflow in syngo Dynamics 9.0, Siemens Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Problem of undesirable behavior in specific reporting workflow in syngo Dynamics 9.0, Siemens Healthcare |
| Manufacturer | Problem of undesirable behavior in specific reporting workflow in syngo Dynamics 9.0, Siemens Healthcare |
| Models | 02.01, 205-2400, 05-10, 23691322, 998-0123, 04F06I2G09, P190-100.691, Q612C09, 12300, 2009.031, 2009.331 |
| Date | Jun 15, 2011 |
| 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