International safety notice

Zdravotnické prostředky pro diagnostiku a terapii zářením

Czech / Ksrzis · CZE · Aug 20, 2020

Key facts

Title Zdravotnické prostředky pro diagnostiku a terapii zářením
Regulator Czech / Ksrzis
Country CZE
Brand Artis zee & Artis Q
Manufacturer Siemens Healthcare GmbH, Německo
Models 91301, 64872105, AX030, 10094137, 213821, V17.OA, AX047, 10094135, 10502504, 2020THE, AX046, 10502502 and 16 more
Event type Safety Notice
Date Aug 20, 2020
Regulator page eregpublicsecure.ksrzis.cz

At a glance

  • No Recall
  • Yes Field safety notice
  • 10–99 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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