International safety notice
Updated Safety Information for the Synthes Trauma External Fixation System (Small, Medium, Distraction Osteogenesis (DO) Ring and Large, Synthes GmbH
Germany / BfArM · DEU · Aug 7, 2014
Key facts
| Title | Updated Safety Information for the Synthes Trauma External Fixation System (Small, Medium, Distraction Osteogenesis (DO) Ring and Large, Synthes GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Synthes Trauma External Fixation System (Small, Medium, Distraction Osteogenesis (DO) Ring and Large, Synthes GmbH |
| Manufacturer | Updated Safety Information for the Synthes Trauma External Fixation System (Small, Medium, Distraction Osteogenesis (DO) Ring and Large, Synthes GmbH |
| Models | FSN20131470, 036.000.182, 036.000.828, 036.000.243, 036.000.389, 036.000.388, 036.000.643, F2503, 036.000.662, 036.000.232, 036.000.555, 036.000.037 and 8 more |
| Date | Aug 7, 2014 |
| 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