Devices

Device Recall Custom Tubing Kit

  • Modèle / numéro de série
    Batch Number 3000020069, UDI Code 10607567203300;  Batch Number 3000021675, UDI Code 10607567203300
  • Classification du dispositif
    Cardiovascular Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The products were distributed to the following US states: AL, OR, and TX.
  • Description du dispositif
    Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 5208 ECC SET, Part Number 701054588
  • Manufacturer
    Datascope Corporation
  • 1 Event

Fabricant

Datascope Corporation
  • Adresse du fabricant
    Datascope Corporation, 15 Law Dr, Fairfield NJ 07004-3206
  • Société-mère du fabricant (2017)
    Getinge AB
  • Source
    USFDA