International safety notice

Information concerning the Corpuls 3 defibrillator from GS Elektromedizinische Geräte

Germany / BfArM · DEU · Oct 22, 2007

Key facts

Title Information concerning the Corpuls 3 defibrillator from GS Elektromedizinische Geräte
Regulator Germany / BfArM
Country DEU
Brand Information concerning the Corpuls 3 defibrillator from GS Elektromedizinische Geräte
Manufacturer Information concerning the Corpuls 3 defibrillator from GS Elektromedizinische Geräte
Models 0660057, 0760071, 0760145, 0760121, 0-86916, 0760143, CORPUIS3, 0760159, 0760097, 0760099, 0660065, 0660060 and 348 more
Date Oct 22, 2007
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

Browse all International device safety notices