Devices

LIFEPAK CR Plus defibrillator

  • Modelo / Serial
    All serial numbers below 31058753
  • Clasificación del producto
    Cardiovascular Devices
  • Clase de dispositivo
    3
  • ¿Implante?
    No
  • Distribución
    The firm distributed units worldwide. Foreign distribution includes Australia, Canada, Costa Rica, Hong Kong, India, Israel, Jamaica, Netherlands, New Zealand, Saudi Arabia, South Africa, Uruguay.
  • Descripción del producto
    LIFEPAK CR Plus defibrillator
  • Manufacturer
    Medtronic Physio Control Corp
  • 1 Event

Fabricante

Medtronic Physio Control Corp
  • Dirección del fabricante
    Medtronic Physio Control Corp, 11811 Willows Rd NE, Redmond WA 98073
  • Source
    USFDA

3 dispositivos con un nombre similar

Más información acerca de la data acá

Physio Control Lifepak CR Plus Defibrillator
  • Modelo / Serial
    Model: Lifepak CR Plus, Affected: Serial numbers manufactured between Aug-2005 and Dec-2012
  • Manufacturer
    Physio-Control Corporation
Lifepak CR Plus defibrillator / Lifepak Express defibrillator
  • Modelo / Serial
  • Descripción del producto
    Medical electronics / Electromedical devices
  • Manufacturer
    Medtronic
Device Recall LIFEPAK CR Plus Defibrillator/Monitor
  • Modelo / Serial
    Serial Numbers: 37026963, 37026983, 37026984, 37026997, 37027002, 37027008, 37027039, 37027040, 37027049, 37027053, 37027063, 37027065, 37027066, 37027070, 37027071, 37027073, 37027075, 37027090, 37027099, 37027105, 37027122, 37027197, 37027529, 37027569, 37031393, 37037850, 37037893, 37037986, 37038002, 37038211, 37038365, 37135986, 37154526 and 37154638.
  • Clasificación del producto
    Cardiovascular Devices
  • Clase de dispositivo
    3
  • ¿Implante?
    No
  • Distribución
    Worldwide Distribution -- US (DC and MN) and Japan.
  • Descripción del producto
    Medtronic Physio-Control LIFEPAK CR Plus Defibrillator/Monitor. || Automated external defibrillator deployed primarily in public access defibrillator environments where the expected use for any one device is once every 20 months. For use on persons requiring defibrillation therapy.
  • Manufacturer
    Physio Control, Inc.