International safety notice
Urgent Safety Notice for the product Tibiagelenkteil, Pol-Endo - size small and medium / Femurgelenkteil, Pol-Endo - size small, Orthodynamics GmbH
Germany / BfArM · DEU · Aug 19, 2014
Key facts
| Title | Urgent Safety Notice for the product Tibiagelenkteil, Pol-Endo - size small and medium / Femurgelenkteil, Pol-Endo - size small, Orthodynamics GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the product Tibiagelenkteil, Pol-Endo - size small and medium / Femurgelenkteil, Pol-Endo - size small, Orthodynamics GmbH |
| Manufacturer | Urgent Safety Notice for the product Tibiagelenkteil, Pol-Endo - size small and medium / Femurgelenkteil, Pol-Endo - size small, Orthodynamics GmbH |
| Models | 22012000, 23093000, 89000-40, 89000-0, 22522000, 23815050, 22022000, 23813000, 23815020, 23815010, 23812000, 23092000 and 3 more |
| Date | Aug 19, 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