CAPI 3 Immunotyping

Fabricant

  • 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
    IGJ

4 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

  • Modèle / numéro de série
  • Description du dispositif
    SEBIA: MINICAP IMMUNOTYPING, CAPILLARYS IMMUNOTYPING, CAPI 3 IMMUNOTYPING
  • Manufacturer
  • Modèle / numéro de série
    PN 2600 | all
  • Description du dispositif
    IVD: Multiple clinical chemistry protein IVD, reagent
  • Manufacturer