International safety notice

Stent de balon expansible Atrium Advanta V12

Spain / AEMPS · ESP · Mar 28, 2022

Key facts

Title Stent de balon expansible Atrium Advanta V12
Regulator Spain / AEMPS
Country ESP
Brand Stent de balon expansible Atrium Advanta V12
Manufacturer Atrium Medical Corporation, EE.UU.
Models 85353, 91.822.52.89, 85330, 85336, 85327, 85354, 33007, V12VER, 85342, 85340, 85323, 85325 and 49 more
Event type Safety Notice
Date Mar 28, 2022

At a glance

  • No Recall
  • Yes Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 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

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