International safety notice

Zdravotnické prostředky pro diagnostiku a terapii zářením

Czech / Ksrzis · CZE · Apr 5, 2017

Key facts

Title Zdravotnické prostředky pro diagnostiku a terapii zářením
Regulator Czech / Ksrzis
Country CZE
Brand Allura Xper Systems, CV20 Systems and UNIQ systems
Manufacturer Philips Medical Systems Nederland B.V.
Models 722022, 98960021599, 722003, 722027, 722010, 722023, 722024, 722031, 722039, 722034, 722015, 722014 and 14 more
Event type Safety Notice
Date Apr 5, 2017
Regulator page eregpublicsecure.ksrzis.cz

At a glance

  • No Recall
  • Yes Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 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