electronic medullary stimulation system

  • Model / Serial
    3660ANS, 3662ANS, specific serials.
  • Product Description
    Neurostimulation system GENESIS: is indicated as an aid in the treatment of chronic pain, not treatable with other therapies of the trunk or extremities including unilateral or bilateral pain associated with any of the following cases: back surgery failure syndrome, as well as low back pain in lower extremities of difficultness. EON / EON MINI neurostimulation system: there are indicated extremities, including unilateral or bilateral pain associated with some of the following cases; syndrome of failure of back surgery, as well as lower back pain and pain in difficult extremities.System MULTIPROGRAM TRIAL STIMULATOR: used for the stimulation of the spinal cord (eme) in the treatment of chronic pain deltronco and extremities, either as an individual palliative method or other types of treatment in the case of multidisciplinary therapy. This modular stimulation system is indicated as an adjuvant in the treatment of chronic refractory pain of the trunk and extremities, including unilateral or bilateral pain associated with angina and chest pain. peripheral vascular disease. Addition of indications for use: "PRODIGY MRI implantable implant model 3772 and PENTA 3228 and OCTRODE 3186 electrodes are conditional magnetic resonance.The use of these devices is conditionally safe in the MRI environment (magnetic resonance imaging) if a complete MRI system is used. and according to the instructions
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “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

One device with a similar name

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  • Model / Serial
    3701, specific lots.
  • Product Description
    Neurostimulation system GENESIS: is indicated as an aid in the treatment of chronic pain, not treatable with other therapies of the trunk or extremities including unilateral or bilateral pain associated with any of the following cases: syndrome of failure of the back surgery, as well as back pain and pain in lower limbs difficult to cure. EON / EON MINI neurostimulation system: are indicated for the treatment of chronic and intractable pain of the trunk and / or extremities, including unilateral or bilateral pain associated with some of the following cases; failure syndrome of back surgery, as well as low back pain and pain in lower limbs difficult to cure. MULTIPROGRAM TRIALSTIMULATOR system: it is used for the stimulation of the spinal cord (eme) in the treatment of chronic trunk pain and extremities, either as an individual palliative method or with other types of treatment in the case of pluridisciplinary therapy. This system of modular stimulation is indicated as adjuvant in the treatment of chronic pain in the trunk and extremities, including unilateral or bilateral pain associated with angina pectoris and peripheral vascular disease.
  • Manufacturer