IMPLANT DIRECT SYBRON MANUFACTURING LLC

14 dispositifs dans la base de données

  • Modèle / numéro de série
    Model Catalog: 423013 (Lot serial: Not specified); Model Catalog: 433010 (Lot serial: Not specified); Model Catalog: 423011 (Lot serial: Not specified)
  • Description du dispositif
    GoDirect Implant Family
  • Modèle / numéro de série
    Model Catalog: 6530-15 (Lot serial: 98151)
  • Description du dispositif
    InterActive Healing Collar
  • Modèle / numéro de série
    Model Catalog: 653211U (Lot serial: 87837)
  • Description du dispositif
    Simply InterActive Implant
  • Modèle / numéro de série
    Model Catalog: 933308 (Lot serial: 73241)
  • Description du dispositif
    Swishtapered Implant
  • Modèle / numéro de série
    Model Catalog: 423013 (Lot serial: 39506); Model Catalog: 423011 (Lot serial: 39506); Model Catalog: 433010 (Lot serial: 60158); Model Catalog: 423013 (Lot serial: 60158); Model Catalog: 423011 (Lot serial: 60158); Model Catalog: 433010 (Lot serial: 54275); Model Catalog: 423013 (Lot serial: 54275); Model Catalog: 423011 (Lot serial: 54275); Model Catalog: 433010 (Lot serial: 51249); Model Catalog: 423013 (Lot serial: 51249); Model Catalog: 423011 (Lot serial: 51249); Model Catalog: 433010 (Lot serial: 44661); Model Catalog: 423013 (Lot serial: 44661); Model Catalog: 423011 (Lot serial: 44661); Model Catalog: 433010 (Lot serial: 54274); Model Catalog: 423013 (Lot serial: 54274); Model Catalog: 423011 (Lot serial: 54274); Model Catalog: 433010 (Lot serial: 40542); Model Catalog: 423013 (Lot serial: 40542); Model Catalog: 423011 (Lot serial: 40542); Model Catalog: 433010 (Lot serial: 39506)
  • Description du dispositif
    GoDirect Implants
9 en plus

13 fabricants avec un nom similaire

En savoir plus sur les données ici

  • 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
8 en plus