International safety notice
Urgent Field Safety Notice for different Certain BellaTek Encode Healing Abutments by Biomet 3i
Germany / BfArM · DEU · Jan 17, 2020
Key facts
| Title | Urgent Field Safety Notice for different Certain BellaTek Encode Healing Abutments by Biomet 3i |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | different Certain BellaTek Encode Healing Abutments |
| Manufacturer | Biomet 3i |
| Models | IEHA456, 1232164, IEHA474, 1229063, IEHA463, 1230640, IEHA354, IEHA344, 1228687, 1227504, 1228701, 1229555 and 61 more |
| Date | Jan 17, 2020 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models 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