International safety notice

Urgent Field Safety Notice for different Certain BellaTek Encode Healing Abutments by Biomet 3i

Germany / BfArM · DEU · Jan 17, 2020

Key facts

Title Urgent Field Safety Notice for different Certain BellaTek Encode Healing Abutments by Biomet 3i
Regulator Germany / BfArM
Country DEU
Brand different Certain BellaTek Encode Healing Abutments
Manufacturer Biomet 3i
Models IEHA456, 1232164, IEHA474, 1229063, IEHA463, 1230640, IEHA354, IEHA344, 1228687, 1227504, 1228701, 1229555 and 61 more
Date Jan 17, 2020
Regulator page bfarm.de

At a glance

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