International safety notice

Koaxialbeatmungsschläuche

Swiss / SwissMedic · CHE · Apr 5, 2023

Key facts

Title Koaxialbeatmungsschläuche
Regulator Swiss / SwissMedic
Country CHE
Brand Koaxialbeatmungsschläuche
Manufacturer Drägerwerk AG & Co. KGaA
Models MP20375, MP01327, MP03374, MP16051, MP02732, MP00333, MP00342, MP01343, MP07207, MP02260, MP07223, MP03383 and 106 more
Event type Safety Notice
Date Apr 5, 2023
Regulator page fsca.swissmedic.ch

At a glance

  • No Recall
  • Yes 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

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