International safety notice
aap Implantate recalls Biorigider Nagel Femur
Germany / BfArM · DEU · Jul 22, 2005
Key facts
| Title | aap Implantate recalls Biorigider Nagel Femur |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | aap Implantate recalls Biorigider Nagel Femur |
| Manufacturer | aap Implantate recalls Biorigider Nagel Femur |
| Models | 0215-30-M, 75019-0, 64083, 929-100, 11-15, 64807, 12099, 929-0, 0217-30-M, 0219-30-M, 12.07.2005, 812290416 and 3 more |
| Date | Jul 22, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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