International safety notice

Zdravotnické prostředky pro jednorázové použití

Czech / Ksrzis · CZE · Apr 16, 2018

Key facts

Title Zdravotnické prostředky pro jednorázové použití
Regulator Czech / Ksrzis
Country CZE
Brand IntraClude™ intra-aortic occlusion device
Manufacturer Edwards Lifesciences LLC
Models 00–17, FCA-93, 10–15, ICF100
Event type Safety Notice
Date Apr 16, 2018
Regulator page eregpublicsecure.ksrzis.cz

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