International safety notice
Safety Notice concerning a corrective action of the defibrillator/pacer SLIM unit, part of the Corpuls3 system, GS Elektromedizinische Geräte G. Stemple GmbH
Germany / BfArM · DEU · Feb 6, 2014
Key facts
| Title | Safety Notice concerning a corrective action of the defibrillator/pacer SLIM unit, part of the Corpuls3 system, GS Elektromedizinische Geräte G. Stemple GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Safety Notice concerning a corrective action of the defibrillator/pacer SLIM unit, part of the Corpuls3 system, GS Elektromedizinische Geräte G. Stemple GmbH |
| Manufacturer | Safety Notice concerning a corrective action of the defibrillator/pacer SLIM unit, part of the Corpuls3 system, GS Elektromedizinische Geräte G. Stemple GmbH |
| Models | 12800103, 04130.2, 65722-22, 2014-02-03, 49-8191-65722-0, 65722, 65722-0, 49-8191-65722-22, D-86916, 13851242, 03-02-2014, CORPULS3 and 1 more |
| Date | Feb 6, 2014 |
| 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