International safety notice

ID-DiaCell I-II

Swiss / SwissMedic · CHE · Oct 10, 2016

Key facts

Title ID-DiaCell I-II
Regulator Swiss / SwissMedic
Country CHE
Brand ID-DiaCell I-II
Manufacturer DiaMed GmbH
Models 45002.66, 45002, 19.Oktober, anti-RH3, 45151.63.1, 45151, 19.10.2016, 31884-440, 24.10.2016, 31884, 4500266.1, ID-DiaAB0 and 14 more
Event type Safety Notice
Date Oct 10, 2016
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