International safety notice
Information about the use of the Amplatzer Septal Occluder from AGA Medical
Germany / BfArM · DEU · Aug 16, 2006
Key facts
| Title | Information about the use of the Amplatzer Septal Occluder from AGA Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Information about the use of the Amplatzer Septal Occluder from AGA Medical |
| Manufacturer | Information about the use of the Amplatzer Septal Occluder from AGA Medical |
| Models | 55427, BOARD2, 12-05-2001, 1998-2001 |
| Date | Aug 16, 2006 |
| 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