Events

Field Safety Notices about Integris H5000 und Integris Allura X-Ray Systems with AD5 table

According to Swiss Agency for Therapeutic Products, this field safety notices involved a device in Switzerland that was produced by Philips Medical Systems BV.

What is this?

Field safety notices are communications sent out by medical device manufacturers or their representatives in relation to actions that they may be taking in relation to their product that is on the market. These are mainly for health workers, but also for users. They can include recalls and alerts.

Learn more about the data here
  • Type of Event
    Field Safety Notice
  • Event ID
    Vk_20070131_08
  • Event Date Posted
    2007-02-13
  • Event Country
    Switzerland
  • Event Source
    SATP
  • Event Source URL
    https://fsca.swissmedic.ch/mep/#?q=Vk_20070131_08
  • Notes / Alerts
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Switzerland.
  • Extra notes in the data

Device

Integris H5000 und Integris Allura X-Ray Systems with AD5 table
  • Model / Serial
    722 018, 722 043, 722 003, 722 005, 722 006, 722 008 | see letter (depends on delivery date)
  • Product Description
    MD: X-ray system, diagnostic, fluoroscopic, angiographic, stationary, digital
  • Manufacturer
    Philips Medical Systems BV

Manufacturer

Philips Medical Systems BV
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    SATP