GE Vingmed Ultrasound AS

4 dispositivos en la base de datos

  • Modelo / Serial
    Model: LOGIQ 9, LOGIQ E9, Vivid 7, Vivid E7, Vivid E9, Vivid E80, Vivid E90, and Vivid E95, Affected:
  • Modelo / Serial
    Model: TEE probe models 6VT-D, 6Tc, 6Tc-RS, 6T, 6T-RS, 9T and 9T-RS, Affected:
  • Modelo / Serial
    Model: , Affected: Vivid E95/E90/E80 with software version 201, revision 54.0 and 61.0, Vivid S70/S60 with software version 201, revision 55.0 and 63.0, Vivid S70N/S60N with software version 201, revision 63.0
  • Modelo / Serial
    Model: , Affected: , Software version: 112.1.0, 112.1.1, 112.1.3

15 fabricantes con un nombre similar

Más información acerca de la data acá

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
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