International safety notice

Getinge Maquet Cardiosave hybrid, Cardiosave rescue IABP - UUENDUS heeliumi indikaatori ebatäpsus ja seadme väljalülitamine aku eemaldamisel

Estonia / EMDDB · EST · Dec 1, 2022

Key facts

Title Getinge Maquet Cardiosave hybrid, Cardiosave rescue IABP - UUENDUS heeliumi indikaatori ebatäpsus ja seadme väljalülitamine aku eemaldamisel
Regulator Estonia / EMDDB
Country EST
Brand Getinge Maquet Cardiosave hybrid, Cardiosave rescue IABP
Manufacturer GETINGE MAQUET CARDIOSAVE HYBRID CARDIOSAVE RESCUE IABP
Models 0002-08-9772, 0998-XX-0800-XX, 07470, 15-20
Date Dec 1, 2022
Regulator page terviseamet.ee

At a glance

  • No Recall
  • No Field safety notice

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