International safety notice
Information concerning the software iPlan Cranial 2.6, iPlan ENT 2.6, iPlan Stereotaxy 2.6 and iPlan Flow 2.6 from BrainLAB
Germany / BfArM · DEU · May 11, 2007
Key facts
| Title | Information concerning the software iPlan Cranial 2.6, iPlan ENT 2.6, iPlan Stereotaxy 2.6 and iPlan Flow 2.6 from BrainLAB |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Information concerning the software iPlan Cranial 2.6, iPlan ENT 2.6, iPlan Stereotaxy 2.6 and iPlan Flow 2.6 from BrainLAB |
| Manufacturer | Information concerning the software iPlan Cranial 2.6, iPlan ENT 2.6, iPlan Stereotaxy 2.6 and iPlan Flow 2.6 from BrainLAB |
| Models | 14-04, OM3-29.US.2, 85622, 85322 |
| Date | May 11, 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