International safety notice

Aplicación del programador del médico para DBS (Estimulación Cerebral Profunda) modelo A610

Spain / AEMPS · ESP · Jul 22, 2021

Key facts

Title Aplicación del programador del médico para DBS (Estimulación Cerebral Profunda) modelo A610
Regulator Spain / AEMPS
Country ESP
Brand Aplicación del programador del médico para DBS (Estimulación Cerebral Profunda) modelo A610
Manufacturer Medtronic Inc., EE.UU.
Models 91.822.52.89, FA968, 28050, 3.0.1057, 3.01062, 28022, 67041, FA969, 3.0.1062, 2021-183, 2.0.4594, SOFTWARE2.0.4584 and 2 more
Event type Safety Notice
Date Jul 22, 2021

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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