International safety notice

Sistemas de Resonancia Magnética Intera, Omniva, Enterprise, Achieva, Achieva XR, Achieva Conversion, Panorama HFO, Ingenia, SmartPath to dStream, Multiva, Prodiva, MR-OR, MR-RT, MR-Linac, MR-Marlin systems.

Spain / AEMPS · ESP · Jan 29, 2019

Key facts

Title Sistemas de Resonancia Magnética Intera, Omniva, Enterprise, Achieva, Achieva XR, Achieva Conversion, Panorama HFO, Ingenia, SmartPath to dStream, Multiva, Prodiva, MR-OR, MR-RT, MR-Linac, MR-Marlin systems.
Regulator Spain / AEMPS
Country ESP
Brand Sistemas de Resonancia Magnética Intera, Omniva, Enterprise, Achieva, Achieva XR, Achieva Conversion, Panorama HFO, Ingenia, SmartPath to dStream, Multiva, Prodiva, MR-OR, MR-RT, MR-Linac, MR-Marlin systems.
Manufacturer PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., HOLANDA
Models “FCO78100484”, FCO78100484, 28050, 49848, 2019-042, 5.416, 91.822.52.89, 28022, FSN78100484, A-28017143, FSN78100484_REF
Event type Safety Notice
Date Jan 29, 2019

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

Browse all International device safety notices