International safety notice

MobileDiagnost wDR

Swiss / SwissMedic · CHE · May 22, 2024

Key facts

Title MobileDiagnost wDR
Regulator Swiss / SwissMedic
Country CHE
Brand MobileDiagnost wDR
Manufacturer Philips Medical Systems DMC GmbH
Models SN18200173, SN18200232, SN190017, SN17200068, SN18200154, SN17200064, 18200048, 16200072, SN17200099, SN17200175, SN19410087, SN17200057 and 749 more
Event type Safety Notice
Date May 22, 2024
Regulator page fsca.swissmedic.ch

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