International safety notice
Safety Notice for Image Diagnost (IDI) MammoWorkstation with a licensed IDI Reporting module, GE Healthcare
Germany / BfArM · DEU · Jul 19, 2011
Key facts
| Title | Safety Notice for Image Diagnost (IDI) MammoWorkstation with a licensed IDI Reporting module, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Image Diagnost (IDI) MammoWorkstation with a licensed IDI Reporting module, GE Healthcare |
| Manufacturer | Safety Notice for Image Diagnost (IDI) MammoWorkstation with a licensed IDI Reporting module, GE Healthcare |
| Models | 12167, 2011-07-06, 53226, V.4.5.3, V.4.5.2, V.4.6.0, V.4.5.0 |
| Date | Jul 19, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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