International safety notice

Urgent Field Safety Notice for MEDUCORE Standard 2 by WEINMANN Emergency Medical Technology GmbH + Co. KG

Germany / BfArM · DEU · Jul 23, 2018

Key facts

Title Urgent Field Safety Notice for MEDUCORE Standard 2 by WEINMANN Emergency Medical Technology GmbH + Co. KG
Regulator Germany / BfArM
Country DEU
Brand MEDUCORE Standard 2
Manufacturer WEINMANN Emergency Medical Technology GmbH + Co. KG
Models 22525, 115967V.A.T, STANDARD², DE35ZZZ00000353971, 115967, 47913245, 24558, 22770, 96-0F, DE288367727, 38144, 96-480 and 1 more
Date Jul 23, 2018
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 10–99 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