Bayer Medical Care

One device in the database

  • Model / Serial
    50856405 50886468 50857510 50886469 50860994 50888285 50866789 50888286 50867921 50888287 50869464 50888288 50869465 50888373 50871131 50890483 50872965 50890484 50878229 50890485 50878230 50892357 50878231 50892358 50878232 50892359 50881328 50892360 50881393 60000321 50881394 60000322 50881395 60000323 50881506 60000692 50881511 60000789 50881512 60000790 50882753 60000833 50886316 60000834 50886467 60000835

24 manufacturers with a similar name

Learn more about the data here

  • Manufacturer Parent Company (2017)
  • Source
    NIDFSINVIMA
  • Manufacturer Parent Company (2017)
  • Source
    MSHM
  • Manufacturer Parent Company (2017)
  • Source
    LAANSM
  • Manufacturer Parent Company (2017)
  • Source
    AEMPSVFOI
  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    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.
  • Source
    IGJ
19 more