Nihon Kohden America, Inc.
7 devices · 60 adverse event reports · 0 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- NA AG-920RAANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE41 reports
- Neuromaster MEE-2000A-DTSTIMULATOR, ELECTRICAL, EVOKED RESPONSE7 reports
- Neuromaster MEE-2000A-LTSTIMULATOR, ELECTRICAL, EVOKED RESPONSE7 reports
- NA GF-210RANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE2 reports
- Life Scope TR MU-671RAMONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)1 report
- NA MU-910RAMONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)1 report
- NK-HealthProtect Wireless Surge Solution A-WSS-002-ZATRANSMITTERS AND RECEIVERS, PHYSIOLOGICAL SIGNAL, RADIOFREQUENCY1 report