International safety notice

Information concerning two defects in Datex-Ohmeda S/5 iCentral software version L-NET05 4.2 from GE Healthcare Technologies

Germany / BfArM · DEU · Nov 3, 2006

Key facts

Title Information concerning two defects in Datex-Ohmeda S/5 iCentral software version L-NET05 4.2 from GE Healthcare Technologies
Regulator Germany / BfArM
Country DEU
Brand Information concerning two defects in Datex-Ohmeda S/5 iCentral software version L-NET05 4.2 from GE Healthcare Technologies
Manufacturer Information concerning two defects in Datex-Ohmeda S/5 iCentral software version L-NET05 4.2 from GE Healthcare Technologies
Models 2005AND, 4.30R, L-NET05
Date Nov 3, 2006
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice

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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

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