International safety notice

Urgent Field Safety Notice for Philips IntelliVue Information Center iX by Philips Medical Systems

Germany / BfArM · DEU · Jan 23, 2018

Key facts

Title Urgent Field Safety Notice for Philips IntelliVue Information Center iX by Philips Medical Systems
Regulator Germany / BfArM
Country DEU
Brand Philips IntelliVue Information Center iX
Manufacturer Philips Medical Systems
Models FSN86201814, 867141, 866117, FSN86201815, 866023, 866389, FSN86201816
Date Jan 23, 2018
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

Browse all International device safety notices