International safety notice

Zdravotnické prostředky pro diagnostiku a terapii zářením

Czech / Ksrzis · CZE · Jul 29, 2015

Key facts

Title Zdravotnické prostředky pro diagnostiku a terapii zářením
Regulator Czech / Ksrzis
Country CZE
Brand Allura Xper Systems
Manufacturer Philips Medical Systems Nederland BV
Models 722022, 722011, THC8AWDS-122, 722025, 72201, 989600-184-665, XCR603-1, FC072200280, 722023, 722012, 989600-184-654, FC072200279 and 5 more
Event type Safety Notice
Date Jul 29, 2015
Regulator page eregpublicsecure.ksrzis.cz

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 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