International safety notice

Aktivní implantabilní zdravotnické prostředky

Czech / Ksrzis · CZE · Sep 30, 2020

Key facts

Title Aktivní implantabilní zdravotnické prostředky
Regulator Czech / Ksrzis
Country CZE
Brand SynchroMed II Clinician Programmer Application
Manufacturer Medtronic Inc.
Models 41171, 241004, 00CZECH, 41-21-802-7000, CT900, 81880264, 41-21-802-7900, 212213, 1.1.342, 17.00, CZ2427000000000081880264, UC201912239EE and 3 more
Event type Safety Notice
Date Sep 30, 2020
Regulator page eregpublicsecure.ksrzis.cz

At a glance

  • No Recall
  • Yes Field safety notice

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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