International safety notice
Information for Corpuls 3 defibrillator, GS Elektromedizinische Geräte
Germany / BfArM · DEU · Jan 18, 2008
Key facts
| Title | Information for Corpuls 3 defibrillator, GS Elektromedizinische Geräte |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corpuls 3 defibrillator, GS Elektromedizinische Geräte |
| Manufacturer | Information for Corpuls 3 defibrillator, GS Elektromedizinische Geräte |
| Models | 2008-01-31, 20-551, D-86916, 2987811, 2008-01-15, 06930, 31.01.2008, 5333236, CH-8953, IR-15338, 390963, 427679 and 63 more |
| Date | Jan 18, 2008 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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