International safety notice

Safety Notice for Brivo OEC 715/785/865 C-Arm systems, GE Healthcare

Germany / BfArM · DEU · Dec 17, 2013

Key facts

Title Safety Notice for Brivo OEC 715/785/865 C-Arm systems, GE Healthcare
Regulator Germany / BfArM
Country DEU
Brand Brivo OEC 715/785/865 C-Arm systems, GE Healthcare
Manufacturer Safety Notice for Brivo OEC 715/785/865 C-Arm systems, GE Healthcare
Models B3S13008, B4S13001, OEC785, B4S13015, OEC715, B2S13001, OEC865, 84116-2862, B3S13005, 15121, B2S13010
Date Dec 17, 2013
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 10–99 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