Devices

ElectriCord

  • Modèle / numéro de série
    Lot numbers 01-08 through 02-16 which are embossed into the power cord metal blades and also those with no lot numbers.
  • Classification du dispositif
    Cardiovascular Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The recalled AC power cords were distributed to approximately 2600 Domestic hospital accounts nationwide and 180 international accounts.
  • Description du dispositif
    Power cord manufactured by ElectriCord Manufacturing Company , P/N 316579, used with DINAMAP Patient Monitors as Follows: DINAMAP PRO Series, DINAMAP PRO 1000 Monitor under both the Critikon and GE Medical Systems. The company name EliectriCord is on the power cord plug.
  • Manufacturer
    GE Medical Systems Information Technologies
  • 1 Event

Fabricant

GE Medical Systems Information Technologies
  • Adresse du fabricant
    GE Medical Systems Information Technologies, 4502 Woodland Corporate Blvd., Tampa FL 33614
  • Source
    USFDA