International safety notice

Corvia Medical

United Kingdom / MHRA · GBR · Sep 18, 2018

Key facts

Title Corvia Medical
Regulator United Kingdom / MHRA
Country GBR
Brand Inter-atrial Shunt Device (IASD) System II/ Corvia Medical, Inc.
Manufacturer Corvia Medical
Models 00261
Event type Safety Notice
Action type Field safety notice
Date Sep 18, 2018
Regulator page gov.uk

At a glance

  • No Recall
  • Yes 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

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