VITEK® 2 Compact 15/30 System


  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    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

3 dispositifs médicaux avec un nom similaire

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  • Modèle / numéro de série
  • Manufacturer
  • Modèle / numéro de série
    Catalog Number: 27415, 27415R, 27530, 27530R, 27630, 27630R
  • Description du dispositif
    Diagnostic medical devices in vitro
  • Manufacturer