Alerte De Sécurité sur Trade name: SOMATOM Computerized Tomography System. Technical name: CT Scanner. . Model: SOMATOM Emotion Registration No .: 10345161972, Risk Class: III; Model: SOMATOM Spirit; Risk Class: III; Registration No: 10345162002 Hazard Class: III. Model: SOMATOM Scope Power, Registration No: 10345161975, Risk Class III :. Model: SOMATOM Perspective, Registration Number: 10345162001, Hazard Class: III

Selon Agência Nacional de Vigilância Sanitária (ANVISA), ce/cet/cette alerte de sécurité concerne un dispositif en/au/aux/à Brazil qui a été fabriqué par Siemens Healthcare Diagnósticos Ltda; Siemens Healthcare GmbH.

Qu'est-ce que c'est?

Les alertes fournissent des informations importantes et des recommandations concernant les dispositifs médicaux. Le fait qu'une alerte soit émise ne signifie pas nécessairement qu'un dispositif soit dangereux. Les alertes de sécurité, qui sont envoyées tant aux travailleurs du secteur médical qu'aux utilisateurs de ces dispositifs, peuvent inclure des rappels. Elles peuvent être rédigées par des fabricants mais aussi par des autorités en charge de la santé.

En savoir plus sur les données ici
  • Type d'événement
    Safety alert
  • ID de l'événement
    2506
  • Date
    2018-03-02
  • Pays de l'événement
  • Source de l'événement
    ANVISA
  • URL de la source de l'événement
  • Notes / Alertes
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 Brazil.
  • Notes supplémentaires dans les données
    The problem described will not occur when using a lateral topogram instead of a topograph or pa. Consequently, we recommend the use of topograms in lateral position for all head acquisitions. If you wish to notify technical complaints and adverse events use the following channels: Notivisa: Notices of adverse events (AE) and technical complaints (QT) for products subject to Sanitary Surveillance should be made through the NOTIVISA System. To access the System, you must register and select the Health Professional option, if you are a liberal professional or the Institution / Entity option, if you are a professional of an institution / entity. Technovigilance System: Patient or citizen can notify through the Technovigilance System / SISTEC access through the link
  • Cause
    Siemens has identified possible incorrect amphole current calculations by the care dose4d algorithm when used on head tomography based on topograms pa (posterior-anterior) or ap.
  • Action
    Field Action Code CT076 / 17 / S & CT077 / 17 / S triggered under the responsibility of Siemens Healthcare Diagnósticos Ltda. The company will send a letter to the customer.

Manufacturer

  • Société-mère du fabricant (2017)
  • Source
    ANVSANVISA