International safety notice
Medical Device Labelling Correction to TomoFix Medial High Tibia Plate, DePuy Synthes/ Swiss
Germany / BfArM · DEU · Dec 6, 2013
Key facts
| Title | Medical Device Labelling Correction to TomoFix Medial High Tibia Plate, DePuy Synthes/ Swiss |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Medical Device Labelling Correction to TomoFix Medial High Tibia Plate, DePuy Synthes/ Swiss |
| Manufacturer | Medical Device Labelling Correction to TomoFix Medial High Tibia Plate, DePuy Synthes/ Swiss |
| Date | Dec 6, 2013 |
| Regulator page | bfarm.deSharedDocs |
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