BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Information for Corpuls 3 defibrillator, GS Elektromedizinische Geräte

Product group Medical electronics / Electromedical devices
Reference 00111/08

GS Elektromedizinische Geräte has issued an information concerning two errors of the Corpuls 3 defibrillator as well as appropriate immediate measures that have to be taken by the users. 1. If the 4-pole-cable is used the device may display an electrical neutral line which could be misinterpreted as an asystoly of the patient. 2. The Monitoring Unit is rebooted unintentionally by start of the realtime printout if the view number 4 is selected. A firmware and a software update are carried out by the manufacturer.

Information for Corpuls 3 defibrillator, GS Elektromedizinische Geräte , Download_VeroeffentlichtAm_EN PDF, 1MB, File does not meet accessibility standards

Use of cookies

Cookies help us to provide our services. By using our website you agree that we can use cookies. Read more about our Privacy Policy and visit the following link: Privacy Policy (only in German)

OK