IMPLANT DIRECT SYBRON MANUFACTURING LLC

14 dispositivos en la base de datos

  • Modelo / Serial
    Model Catalog: 423013 (Lot serial: Not specified); Model Catalog: 433010 (Lot serial: Not specified); Model Catalog: 423011 (Lot serial: Not specified)
  • Descripción del producto
    GoDirect Implant Family
  • Modelo / Serial
    Model Catalog: 6530-15 (Lot serial: 98151)
  • Descripción del producto
    InterActive Healing Collar
  • Modelo / Serial
    Model Catalog: 653211U (Lot serial: 87837)
  • Descripción del producto
    Simply InterActive Implant
  • Modelo / Serial
    Model Catalog: 933308 (Lot serial: 73241)
  • Descripción del producto
    Swishtapered Implant
  • Modelo / Serial
    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)
  • Descripción del producto
    GoDirect Implants
9 más

13 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.
  • Source
    IGJ
8 más