International safety notice

Equipos de resonancia magnética 3T: Ingenia Elition X, Ingenia Elition S, SmartPath a Ingenia Elition X, MR 7700 y Actualización a MR 7700

Spain / AEMPS · ESP · Apr 21, 2023

Key facts

Title Equipos de resonancia magnética 3T: Ingenia Elition X, Ingenia Elition S, SmartPath a Ingenia Elition X, MR 7700 y Actualización a MR 7700
Regulator Spain / AEMPS
Country ESP
Brand Equipos de resonancia magnética 3T: Ingenia Elition X, Ingenia Elition S, SmartPath a Ingenia Elition X, MR 7700 y Actualización a MR 7700
Manufacturer Philips Healthcare, Países Bajos
Models 62024, 45567, 46069, 45058, 45411, 781358, 46003, 2022-544, 42085, 45095, 45564, 46214 and 475 more
Event type Safety Notice
Date Apr 21, 2023

At a glance

  • No Recall
  • Yes Field safety notice
  • 100–999 Matching device models in FDA data
  • 100–999 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