Advanced Neuromodulation Systems, Inc.

5 dispositifs dans la base de données

  • Modèle / numéro de série
    3701, 3711 | all
  • Description du dispositif
    AIMD: Pacemaker battery charger
  • Modèle / numéro de série
    all | all
  • Description du dispositif
    MD: Neural-tissue electrical stimulation lead
  • Modèle / numéro de série
    65-3788 | All
  • Description du dispositif
    AIMD: Pacemaker battery charger; Spinal cord electrical stimulation system, analgesic
  • Modèle / numéro de série
    3719, 3721 | All
  • Description du dispositif
    AIMD: Pacemaker battery charger; Spinal cord electrical stimulation system, analgesic
  • Modèle / numéro de série
    3224, 3243, 3246, 3266, 3267, 3268, 3269, 3283, 3286, 3208, 3210, 3219, 3214, 3240, 3254, 3255, 3244, 3262, 3263, 3245, 3264, 3265, 3280, 3288, 3289, 3228
  • Description du dispositif
    MD: Neural-tissue electrical stimulation lead

Un fabricant avec un nom similaire

En savoir plus sur les données ici

  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    NIDFSINVIMA