Pulsar-18

Fabricant

  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    Biotronik told ICIJ that, when it identifies the need to issue a recall, the company immediately informs physicians of all potentially affected patients. It also noted that product recalls for all manufactures are publically available on the relevant national authorities’ websites. “As soon as an event is deemed serious either by a hospital or a manufacturer, it is reported inter alia to the regulatory authority in the country in which the incidence has occurred, as well as to the FDA for US-approved devices, even if the event has occurred outside of the US,” the company said.
  • Source
    VNSAWH

17 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

  • Modèle / numéro de série
    Model: Product Codes: 366812, 366817, 366822, 366827, 366832, 366837, 366842, 366847, Affected: Selected lots
  • Manufacturer
  • Modèle / numéro de série
  • Description du dispositif
    md
  • Manufacturer
  • Modèle / numéro de série
  • Description du dispositif
    medical_device
  • Manufacturer
12 en plus