International safety notice
Corrective Action of MEE-1000A Neuromaster, Nihon Kohden
Germany / BfArM · DEU · Jan 6, 2012
Key facts
| Title | Corrective Action of MEE-1000A Neuromaster, Nihon Kohden |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corrective Action of MEE-1000A Neuromaster, Nihon Kohden |
| Manufacturer | Corrective Action of MEE-1000A Neuromaster, Nihon Kohden |
| Models | MEE-1000A, JB-116B, JB-132B, MS-110B |
| Date | Jan 6, 2012 |
| 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