Proteus 235

Manufacturer

  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    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

13 devices with a similar name

Learn more about the data here

  • Model / Serial
    Code/Serial Numbers: PAT.003, PAT.006, PAT.107, PAT.108, PAT.109, PAT.110, PAT.111, PAT.112, PAT.113, PAT.114, PAT.115, SAT.116, SAT.117, SAT.119, SAT.120, SAT.122, SAT.123 and SAT.126
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Products distributed to FL, VA, PA, OK, IL, NJ, WA, TN, LA, TX, South Korea, Germany, France, Czech Republic, Italy, Poland, and Sweden
  • Product Description
    Proteus 235 and Proteus ONE proton therapy systems
  • Manufacturer
  • Model / Serial
  • Product Description
    Radiotherapy / Radiation protection - nuclear medical therapeutic equipment
  • Manufacturer
  • Model / Serial
    Model Number: Proteus ONE a Proteus PLUS (Proteus 235) a adaPT insight (I2C) Serial Number: PAT.000, PAT.003, PAT.006, PAT.107, PAT.108, PAT.109, PAT.110, PAT.111, PAT.112, PAT.113, PAT.114, PAT.115, SAT.116, SAT.117, SAT.119, SAT.120, SAT.122, SAT.123, SAT.126, SBF.101
  • Product Description
    Medical devices for diagnostics and radiation therapy
  • Manufacturer
  • Model / Serial
  • Product Description
    Proteus 235, Ion Beam Applications S.A.
  • Manufacturer
8 more