SW 8870MMC01 NVISION INTSTM ENTERRA2


Product Overview

SW 8870MMC01 NVISION INTSTM ENTERRA2
N'VISION® - 8870MMC01


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 Temperature - Degrees Celsius
    • 57.00
    • -34.00
  • Storage Environment Temperature - Degrees Fahrenheit
    • 135.00
    • -30.00

  • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    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: 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: 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


    Device Identifiers

    Device Id: 00763000129514

    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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