International safety notice
Information concerning the iPlan RT Dose 3.0, iPlan RT Dose 3.0.1 und iPlan RT Dose 3.0.2. from BrainLAB
Germany / BfArM · DEU · Apr 30, 2007
Key facts
| Title | Information concerning the iPlan RT Dose 3.0, iPlan RT Dose 3.0.1 und iPlan RT Dose 3.0.2. from BrainLAB |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Information concerning the iPlan RT Dose 3.0, iPlan RT Dose 3.0.1 und iPlan RT Dose 3.0.2. from BrainLAB |
| Manufacturer | Information concerning the iPlan RT Dose 3.0, iPlan RT Dose 3.0.1 und iPlan RT Dose 3.0.2. from BrainLAB |
| Models | 3RATNLAB, 3.0.1, IPLÜ1, 85822, IP12T, 85622, 3.0.2 |
| Date | Apr 30, 2007 |
| 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