International safety notice

Urgent Medical Device Correction Notification for the NicoletOne Software v5.94, Natus Neurology lncorporated

Germany / BfArM · DEU · Oct 9, 2015

Key facts

Title Urgent Medical Device Correction Notification for the NicoletOne Software v5.94, Natus Neurology lncorporated
Regulator Germany / BfArM
Country DEU
Brand the NicoletOne Software v5.94, Natus Neurology lncorporated
Manufacturer Urgent Medical Device Correction Notification for the NicoletOne Software v5.94, Natus Neurology lncorporated
Date Oct 9, 2015
Regulator page bfarm.deSharedDocs

At a glance

  • No Recall
  • No 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

Browse all International device safety notices