Events

Field Safety Notices about ADVIA Centaur Calibrator 30

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 Siemens Healthcare Diagnostics Inc.

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
    1178
  • Date
    2017-06-30
  • 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

ADVIA Centaur Calibrator 30
  • Model / Serial
    Catalog Number: SMN 10379810 (2PK); 10379811 (6PK); 10697756 (Ref 2PK) Batch Number: SMN 10379810 00387A21 16673A21 36243A21 SMN 10379811 00388A21 15448A21 51211A21 SMN 10697756 20640A21 51024A21
  • Product Description
    Diagnostic medical devices in vitro
  • Manufacturer
    Siemens Healthcare Diagnostics Inc

Manufacturer

Siemens Healthcare Diagnostics Inc
  • Manufacturer Parent Company (2017)
    Siemens Ag
  • Source
    MHSIDCCCDMIS