International safety notice
Safety Notice for Varian Clinac® accelerators with Mark or Millennium MLC and BrainLAB m3 MLC, Varian medical systems
Germany / BfArM · DEU · Feb 29, 2012
Key facts
| Title | Safety Notice for Varian Clinac® accelerators with Mark or Millennium MLC and BrainLAB m3 MLC, Varian medical systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Varian Clinac® accelerators with Mark or Millennium MLC and BrainLAB m3 MLC, Varian medical systems |
| Manufacturer | Safety Notice for Varian Clinac® accelerators with Mark or Millennium MLC and BrainLAB m3 MLC, Varian medical systems |
| Models | H535122, H535168, 1.888.VARIAN5, H534015, H530204, H530023, H535111, H535199, H535058, H535009, H535085, CP-05591 and 200 more |
| Date | Feb 29, 2012 |
| 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