International safety notice
Safety Notice and Update for control units MICROSPEED UNI / ARTHRO, Aesculap
Germany / BfArM · DEU · Dec 16, 2010
Key facts
| Title | Safety Notice and Update for control units MICROSPEED UNI / ARTHRO, Aesculap |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | control units MICROSPEED UNI / ARTHRO, Aesculap |
| Manufacturer | Safety Notice and Update for control units MICROSPEED UNI / ARTHRO, Aesculap |
| Models | GD678, 726261, 78S32, GD675I, GD674, 2010-11-05, DEUTS01E, GD684, GD665, GD679, 65109852, GD670 and 7 more |
| Date | Dec 16, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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