sinus-SuperFlex-635

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

10 devices with a similar name

Learn more about the data here

  • Model / Serial
  • Product Description
    medical_device
  • Manufacturer
  • Model / Serial
    8606-6200/ sinus-SuperFlex-635, Stent system, 6x200 mm, 6F/ 75 cm, .035i, application device 8606-7200/ sinus-SuperFlex-635, Stent system, 6x200 mm, 6F/ 120 cm, .035i, application device 8607-6200/ sinus-SuperFlex-635, Stent system, 7x200 mm, 6F/ 75 cm, .035i, application device 8607-7200/ sinus-SuperFlex-635, Stentsystem, 7x200 mm, 6F/ 120 cm, .035i, application device
  • Manufacturer
  • Model / Serial
    Catalog Number: 8606-6200 8606-7200 8607-6200 8607-7200 Model Number: sin-SF-635-v/b-06x200-75 sin-SF-635-v/b-06x200-120 sin-SF-635-v/b-07x200-75 sin-SF-635-v/b-07x200-120 Batch Number: viz příloha: dotčené šarže
  • Product Description
    Inactive implantable medical devices
  • Manufacturer
5 more