International safety notice

Plataforma del sistema de injerto de stent abdominal Ovation: Injerto de stent abdominal Ovation Prime™ y Injerto de stent del cuerpo aórtico Ovation iX

Spain / AEMPS · ESP · Oct 22, 2018

Key facts

Title Plataforma del sistema de injerto de stent abdominal Ovation: Injerto de stent abdominal Ovation Prime™ y Injerto de stent del cuerpo aórtico Ovation iX
Regulator Spain / AEMPS
Country ESP
Brand Plataforma del sistema de injerto de stent abdominal Ovation: Injerto de stent abdominal Ovation Prime™ y Injerto de stent del cuerpo aórtico Ovation iX
Manufacturer TriVascular Inc, subsidiaria de Endologix Inc. EEUU.
Models LOCAL3, TV-AB2380-D, 36001, 3INCLUYE, TV-AB2680-D, TV-AB2080-I, TV-AB3480-D.INJERTO, 48093, QKGBZKY9F8, TV-AB3480-D, 95403, TV-AB2380-I and 17 more
Event type Safety Notice
Date Oct 22, 2018

At a glance

  • No Recall
  • Yes Field safety notice
  • 10–99 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