MONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM)

FDA product code DRT · Class 2 · 7 devices · 395 reports · 3 deaths reported · 1 devices named in recalls

• NA ZM-531PA

  Nihon Kohden Corporation · MONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM)
  1 death167 reports
• NA B155 VSP3.0 Patient Monitor

  GE Medical Systems Information Technologies, Inc. · MONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM)
  2 recalls0 reports
• NA ZM-530PA

  Nihon Kohden Corporation · MONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM)
  2 deaths93 reports
• NA ZM-521PA

  Nihon Kohden Corporation · MONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM)
  79 reports
• NA ZM-520PA

  Nihon Kohden Corporation · MONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM)
  24 reports
• NA ZM-541PA

  Nihon Kohden Corporation · MONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM)
  22 reports
• NA ZM-540PA

  Nihon Kohden Corporation · MONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM)
  10 reports