International safety notice

Artelac Rebalance EDO /Artelac Rebalance SDU

Swiss / SwissMedic · CHE · Nov 14, 2018

Key facts

Title Artelac Rebalance EDO /Artelac Rebalance SDU
Regulator Swiss / SwissMedic
Country CHE
Brand Artelac Rebalance EDO /Artelac Rebalance SDU
Manufacturer Dr. Gerhard Mann chem.-pharm. Fabrik GmbH
Models 090949094, 09722545, 13581, 165‐173, 3093518, 779146, 779167, 07.12.2018
Event type Safety Notice
Date Nov 14, 2018
Regulator page fsca.swissmedic.ch

At a glance

  • No Recall
  • Yes 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