International safety notice
Safety Notice for semi-automated external defibrillators cardioLife AED, Nihon Kohden
Germany / BfArM · DEU · Apr 14, 2011
Key facts
| Title | Safety Notice for semi-automated external defibrillators cardioLife AED, Nihon Kohden |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | semi-automated external defibrillators cardioLife AED, Nihon Kohden |
| Manufacturer | Safety Notice for semi-automated external defibrillators cardioLife AED, Nihon Kohden |
| Models | DE34500100600041740609, 573-19, DE76300107000000607438, 01-15, 50010060, XX.04.2011, 81618021, 27-599, 573-0, 06003, AED-2100K, 033203 and 4 more |
| Date | Apr 14, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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