International safety notice

Zdravotnické prostředky pro diagnostiku a terapii zářením

Czech / Ksrzis · CZE · Apr 30, 2018

Key facts

Title Zdravotnické prostředky pro diagnostiku a terapii zářením
Regulator Czech / Ksrzis
Country CZE
Brand Allura Xper / UNIQ
Manufacturer Philips Medical Systems Nederland B.V.
Models 722019, 722005, 722026, 8.2.27, 8.1.25.5, 1.0.10, 722011, 8.2.25.0, 722015, 722033, 8.2.25.O, 722038 and 26 more
Event type Safety Notice
Date Apr 30, 2018
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