International safety notice
Safety Notice concerning use of Brainlab Scull Reference Base in combination with KLS Martin Cross-Drive screws, Brainlab AG
Germany / BfArM · DEU · Aug 22, 2011
Key facts
| Title | Safety Notice concerning use of Brainlab Scull Reference Base in combination with KLS Martin Cross-Drive screws, Brainlab AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Safety Notice concerning use of Brainlab Scull Reference Base in combination with KLS Martin Cross-Drive screws, Brainlab AG |
| Manufacturer | Safety Notice concerning use of Brainlab Scull Reference Base in combination with KLS Martin Cross-Drive screws, Brainlab AG |
| Models | 52128, BL-IL-52121B_52129-REV1.0, 52129, 52129A, 11-02-18.TGE.1, 85622, 52170, 25-678-06, 52121B, 25-878-06-09, BL-IL-60903-79-REV2.0, 14-04 |
| Date | Aug 22, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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