Events

Field Safety Notices about ARTIS Q

According to Swiss Agency for Therapeutic Products, this field safety notices involved a device in Switzerland that was produced by Siemens AG, Healthcare Sector, Buisness Unit AX.

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_20141223_21
  • Event Date Posted
    2015-01-12
  • Event Country
    Switzerland
  • Event Source
    SATP
  • Event Source URL
    https://fsca.swissmedic.ch/mep/#?q=Vk_20141223_21
  • 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

ARTIS Q
  • Model / Serial
    Artis Q ceilingSeriennummernband 109000 bis 109091ArtisQ.zen ceiling Seriennummernband 111000bis 111005Artis Q ceiling serial number range109000 to 109091 Artis Q.zen ceiling serialnumber range 111000 to 111005
  • Product Description
    MD: Stationary angiographic x-ray system, digital
  • Manufacturer
    Siemens AG, Healthcare Sector, Buisness Unit AX

Manufacturer

Siemens AG, Healthcare Sector, Buisness Unit AX