PROGRAMMER 8840 CLINICIAN REFURB US


Product Overview

PROGRAMMER 8840 CLINICIAN REFURB US
N'VISION™ - 8840-RFB


Device Description

An external, portable, non-dedicated, electrically-powered device intended to change, noninvasively (i.e., wirelessly), the operating parameters (programs) of multiple types of implanted electronic devices (e.g., multiple types of pulse generators); it may in addition program the external trial device used prior to the implanted one. It includes controls (e.g., graphical user interface), integrated software, and a wireless communication transmitter and receiver. It typically also provides historic and/or current information regarding the performance of the implant.


Environmental Conditions

  • Storage Environment Humidity - Percent (%) Relative Humidity
    • 75.00
    • 30.00
  • Storage Environment Temperature - Degrees Celsius
    • 65.00
    • -40.00
  • Storage Environment Temperature - Degrees Fahrenheit
    • 149.00
    • -40.00

  • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: LGW

    Device Name: Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    Device Class: 3

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 2

    Review Panel: NE

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: N/A

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Code: NHL

    Device Name: Stimulator, Electrical, Implanted, For Parkinsonian Symptoms

    Device Class: 3

    Physical State: N/A

    Definition: Bilateral stimulation of the internal globus pallidus (GPi) or the subthalamic nucleus (STN) using Medtronic Activa Parkinson's Control Therapy is indicated for adjunctive therapy in reducing some of the symptoms of advanced, levodopa-responsive Parkinsons disease that are not adequately controlled with medication.

    Submission Type ID: 2

    Review Panel: NE

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: N/A

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Code: OLM

    Device Name: Deep Brain Stimulator For Obsessive Compulsive Disorder (Ocd)

    Device Class: f

    Physical State: Electrodes, extension and IPG

    Definition: The device is indicated for bilateral stimulation of the anterior limb of the internal capsule, this device is indicated as an adjunct to medications and as an alternative to anterior capsulotomy for treatment of chronic, severe, treatment-resistant Obsessive Compulsive Disorder (OCD) in adult patients who have failed at least three Selective Serotonin Reuptake Inhibitors (SSRIs).

    Submission Type ID: 6

    Review Panel: NE

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: Deep brain stimulation

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: Anterior limb of the internal capsule in the brain

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Code: MHY

    Device Name: Stimulator, Electrical, Implanted, For Parkinsonian Tremor

    Device Class: 3

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 2

    Review Panel: NE

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: N/A

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Code: PJS

    Device Name: Stimulator, Electrical, Implanted, For Essential Tremor

    Device Class: 3

    Physical State: System components include implantable pulse generator, leads, extensions, patient programmer, and charger

    Definition: Deep Brain Stimulation for the treatment of essential tremor

    Submission Type ID: 2

    Review Panel: NE

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: Implantable pulse generator will produce electrical pulses which will stimulate deep brain structures through electrodes on leads.

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: Deep Brain Structures

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Code: QON

    Device Name: Implanted Electrical Device Intended For Treatment Of Fecal Incontinence

    Device Class: 3

    Physical State: Receiver implanted in the abdomen with electrodes for pulsed-stimulation that are implanted either in the bladder wall or in the pelvic floor, and a battery-powered transmitter outside the body

    Definition: Treatment of chronic fecal incontinence

    Submission Type ID: 2

    Review Panel: GU

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: Electrical stimulation of the sacral nerve

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: Sacral nerve, bladder, urinary and anal sphincters, pelvic floor, and rectosigmoid colon

    Regulation Number: 876.5270

    Third Party Flag: N

    Medical Specialty: GU


    Code: EZW

    Device Name: Stimulator, Electrical, Implantable, For Incontinence

    Device Class: 3

    Physical State: N/A

    Definition: PMAs to be filed by 12/26/96 (61 FR 50707 (9/27/96))

    Submission Type ID: 2

    Review Panel: GU

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: N/A

    Regulation Number: 876.5270

    Third Party Flag: N

    Medical Specialty: GU


    Code: LKK

    Device Name: Pump, Infusion, Implanted, Programmable

    Device Class: 3

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 2

    Review Panel: HO

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: N/A

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Code: LNQ

    Device Name: Intestinal Stimulator

    Device Class: f

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 6

    Review Panel: GU

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: N/A

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Code: MRU

    Device Name: Implanted Subcortical Electrical Stimulator (Motor Disorders)

    Device Class: f

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 6

    Review Panel: NE

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: N/A

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Device Identifiers

    Device Id: 00763000875862

    Device Type: Primary

    DeviceId Issuing Agency: GS1

    Contains DI Number: N/A

    Package Quantity: N/A

    Package Discontinue Date: N/A

    Package Status: N/A

    Package Type: N/A


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