International safety notice

Urgent Field Safety Notice for Ellipse VR, Ellipse DR by S.. Jude Medical CRMD

Germany / BfArM · DEU · Jul 11, 2019

Key facts

Title Urgent Field Safety Notice for Ellipse VR, Ellipse DR by S.. Jude Medical CRMD
Regulator Germany / BfArM
Country DEU
Brand Ellipse VR, Ellipse DR
Manufacturer S.. Jude Medical CRMD
Models 15900, CD1377-36QC, 25852, CD2377-36C, 91342, 46-8474-4147, CD2377-36QC, 37265, CD1377-36C
Date Jul 11, 2019
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 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