International safety notice
Safety Information concerning the Proteus XR/a, Revolution XR/d and Definium 8000 X-ray systems from GE Healthcare
Germany / BfArM · DEU · Dec 21, 2006
Key facts
| Title | Safety Information concerning the Proteus XR/a, Revolution XR/d and Definium 8000 X-ray systems from GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Safety Information concerning the Proteus XR/a, Revolution XR/d and Definium 8000 X-ray systems from GE Healthcare |
| Manufacturer | Safety Information concerning the Proteus XR/a, Revolution XR/d and Definium 8000 X-ray systems from GE Healthcare |
| Models | PICTURE2, 2259988, 5177923-100, 53201-0414 |
| Date | Dec 21, 2006 |
| 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