Events

Field Safety Notices about Foot Control S-N1 / S-N2

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 W&H Dentalwerk Bürmoos GmbH.

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
    1421
  • Date
    2018-01-25
  • 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

Foot Control S-N1 / S-N2
  • Model / Serial
    Model Number: 05046200, 05046211, 05046210, 06202400, 30285000, 30285001 Serial Number: 05046200 SN v. 22400 - 23429 and E02201 - E02485 05046211 SN v. E01011 - E01033 05046210 SN v. E01035 - E01071 06202400 SN v. 24315 - 34040 and E01358 - E01658 30285000 SN v. 01001 - 02318 30285001 SN v. 01001 - 02318
  • Product Description
    Dental medical devices
  • Manufacturer
    W&H Dentalwerk Bürmoos GmbH

Manufacturer

W&H Dentalwerk Bürmoos GmbH