International safety notice

Urgent Field Safety Notice for Artelac Rebalance EDO /Artelac Rebalance SDU by Dr. Gerhard Mann Chem. Pharm. Fabrik

Germany / BfArM · DEU · Nov 16, 2018

Key facts

Title Urgent Field Safety Notice for Artelac Rebalance EDO /Artelac Rebalance SDU by Dr. Gerhard Mann Chem. Pharm. Fabrik
Regulator Germany / BfArM
Country DEU
Brand Artelac Rebalance EDO /Artelac Rebalance SDU
Manufacturer Dr. Gerhard Mann Chem. Pharm. Fabrik
Models 01805, 13581, 07.12.2018, 090949094, 779146, 165-173, 779167
Date Nov 16, 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