International safety notice
Recall for MDI Hybrid Implants with O-Ball Abutment, IMTEC
Germany / BfArM · DEU · Jul 22, 2009
Key facts
| Title | Recall for MDI Hybrid Implants with O-Ball Abutment, IMTEC |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | MDI Hybrid Implants with O-Ball Abutment, IMTEC |
| Manufacturer | Recall for MDI Hybrid Implants with O-Ball Abutment, IMTEC |
| Models | 3503093-19, 35209256, 3502092-56, MIL-OB13, M11-0B13, MLL.OB16, MLL.OB15, 3602092-56, MIL-OB15, MII-OB13, 3503092-43, 06171 and 4 more |
| Date | Jul 22, 2009 |
| Regulator page | bfarm.de |
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