Field Safety Notices about G210 Invicell CO2/O2 Incubator, Standard and Plus

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 Kivex Biotex A/S.

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
    730
  • Date
    2016-09-06
  • Event Country
  • Event Source
    MHSIDCCCDMIS
  • Event Source URL
  • 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

  • Model / Serial
    Catalog Number: 59500, 60000 Model Number: Model Standard, Model Plus Serial Number: 1606G210B300020 1606G210B200203 1606G210B200201 1606G210B200200 1606G210A140146 1605G210B300011 1604G210B300009 1605G210A140145 1605G210A140144 1605G210A140142 1605G210A140143 1605G210A130139 1605G210A130138 1604G210B300008 1604G210B300007 1604G210B300006 1604G210A130137 1604G210A130136 1604G210A130135 1604G210A130134 1604G210A130133 1603G210A130131 1603G210A130130 1603G210A120129
  • Product Description
    Electromechanical medical devices
  • Manufacturer

Manufacturer