Devices

Revision K Actuator Test Boards

  • Modèle / numéro de série
    Revision K Actuator Test Boards
  • Classification du dispositif
    Gastroenterology-Urology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    USA (nationwide) and the country of Canada.*
  • Description du dispositif
    Revision K Actuator Test Boards sold as replacement parts for use with Fresenius 2008-Series Hemodialysis Machines (2008K, 2008K2, 2008K@home and 2008T). || Part Number: 190713 Revision K
  • Manufacturer
    Fresenius Medical Care Holdings, Inc.
  • 1 Event

Fabricant

Fresenius Medical Care Holdings, Inc.
  • Adresse du fabricant
    Fresenius Medical Care Holdings, Inc., 920 Winter St, Waltham MA 02451-1521
  • Société-mère du fabricant (2017)
    Fresenius SE & Co KGaA
  • Source
    USFDA