International safety notice
Software-upgrade regarding the device NicoletOne Software v5.60.2 through v5.71. with Cortical Stimulator License, Nicolet™ Cortical Stimulator Control Unit and the Nicolet C64 SSU Amplifier, CareFusion
Germany / BfArM · DEU · Oct 26, 2011
Key facts
| Title | Software-upgrade regarding the device NicoletOne Software v5.60.2 through v5.71. with Cortical Stimulator License, Nicolet™ Cortical Stimulator Control Unit and the Nicolet C64 SSU Amplifier, CareFusion |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Software-upgrade regarding the device NicoletOne Software v5.60.2 through v5.71. with Cortical Stimulator License, Nicolet™ Cortical Stimulator Control Unit and the Nicolet C64 SSU Amplifier, CareFusion |
| Manufacturer | Software-upgrade regarding the device NicoletOne Software v5.60.2 through v5.71. with Cortical Stimulator License, Nicolet™ Cortical Stimulator Control Unit and the Nicolet C64 SSU Amplifier, CareFusion |
| Models | 608-829-8517, 800-356, 608.441.2330, 829-8500, V5.60.2, 356-0007, V5.60.25.71.4, 5.71.4, 44994, 800.356.0007, 53562, 5.71.5 and 7 more |
| Date | Oct 26, 2011 |
| Regulator page | bfarm.de |
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