International safety notice

Uroskop Omnia Max

Swiss / SwissMedic · CHE · Sep 25, 2020

Key facts

Title Uroskop Omnia Max
Regulator Swiss / SwissMedic
Country CHE
Brand Uroskop Omnia Max
Manufacturer Siemens Healthcare GmbH, Diagnostic Imaging, X-Ray-Products
Models 024-20-S, CH-8047, 24.09.2020, 91301, XP006, 64872105, XP026, 10999410, 10762473, 18-4084, 213821, XP024
Event type Safety Notice
Date Sep 25, 2020
Regulator page fsca.swissmedic.ch

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching device models 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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