Devices

Device Recall Custom Tubing Kit

  • Modelo / Serial
    Batch Number 3000020069, UDI Code 10607567203300;  Batch Number 3000021675, UDI Code 10607567203300
  • Clasificación del producto
    Cardiovascular Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    The products were distributed to the following US states: AL, OR, and TX.
  • Descripción del producto
    Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 5208 ECC SET, Part Number 701054588
  • Manufacturer
    Datascope Corporation
  • 1 Event

Fabricante

Datascope Corporation
  • Dirección del fabricante
    Datascope Corporation, 15 Law Dr, Fairfield NJ 07004-3206
  • Empresa matriz del fabricante (2017)
    Getinge AB
  • Source
    USFDA