Events

Field Safety Notices about Aespire 7900 Anesthesia Devices, Aespire View, Aestiva 7900, Aestiva MRI, Aisys, Aisys CS2, Avance and Avance CS2

According to Ministry of Health, State Institute for Drug Control, Coordination Center for Departmental Medical Information Systems, this field safety notices involved a device in Czechia that was produced by Datex-Ohmeda, Inc. (GE Healthcare).

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
    378
  • Date
    2016-01-22
  • Event Country
    Czechia
  • Event Source
    MHSIDCCCDMIS
  • Event Source URL
    https://eregpublicsecure.ksrzis.cz/Registr/RZPRO/FSN
  • Notes / Alerts
    Czech data is current through July 2018. All of the data comes from the Czech Public Registry of Medical Devices, 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 data from the U.S. and the Czech Republic.
  • Extra notes in the data

Device

Aespire 7900 Anesthesia Devices, Aespire View, Aestiva 7900, Aestiva MRI, Aisys, Aisys CS2, Avanc...
  • Model / Serial
    Batch Number: Zařízení, která byla odeslána z výrobního centra společnosti GE Healthcare a instalována od 20. dubna 2015 do konce října 2015
  • Product Description
    Anesthetic and respiratory medical devices
  • Manufacturer
    Datex-Ohmeda, Inc. (GE Healthcare)

Manufacturer

Datex-Ohmeda, Inc. (GE Healthcare)