International safety notice
Information for the GAMMAMED plus-, the GAMMAMED plus 3/24- and the MAMMOSOURCE-Afterloading devices, Varian
Germany / BfArM · DEU · May 12, 2006
Key facts
| Title | Information for the GAMMAMED plus-, the GAMMAMED plus 3/24- and the MAMMOSOURCE-Afterloading devices, Varian |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the GAMMAMED plus-, the GAMMAMED plus 3/24- and the MAMMOSOURCE-Afterloading devices, Varian |
| Manufacturer | Information for the GAMMAMED plus-, the GAMMAMED plus 3/24- and the MAMMOSOURCE-Afterloading devices, Varian |
| Models | 070605 |
| Date | May 12, 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