Manufacturers

ADAC Laboratories

5 dispositifs dans la base de données

Device Recall Pinnacle3
  • Modèle / numéro de série
    Version 6.4a, Rev. A
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China, and Korea.
  • Description du dispositif
    Philips Pinnacle3 Version 6.4a Radiation Therapy Planning Software CD, Part Number 9104-0121B, Rev. A
Device Recall Pinnacle3
  • Modèle / numéro de série
    Version 6.6c, Rev. A
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China, and Korea.
  • Description du dispositif
    Pinnacle3 Radiation Therapy Planning System, Version 6.6c CD, Part Number 9104-0121C Rev. A
Device Recall Pinnacle3
  • Modèle / numéro de série
    Version 7.0e, Rev. A
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China, and Korea.
  • Description du dispositif
    Pinnacle3 Radiation Therapy Planning System, Version 7.0e CD, Part Number Part # 9104-2011A Rev. A
Device Recall Pinnacle3
  • Modèle / numéro de série
    Version 6.6c
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China, and Korea.
  • Description du dispositif
    Pinnacle3 Radiation Therapy Planning System, Version 6.6c Kit, Model Number 9200-0613C-ENG
Device Recall Pinnacle3
  • Modèle / numéro de série
    Version 7.0e
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China, and Korea.
  • Description du dispositif
    Pinnacle3 Radiation Therapy Planning System, Version 7.0e Kit, Model Number 9200-9052A-ENG

Un fabricant avec un nom similaire

En savoir plus sur les données ici

Philips Medical Systems Ltda.; ADAC Laboratories (A Philips Medical Systems Company)
  • Société-mère du fabricant (2017)
    Philips
  • Source
    ANVSANVISA