CABLE 5832S GLBL SMALL CLIP


Product Overview

CABLE 5832S GLBL SMALL CLIP
NA - 5832S


Device Description

A non-patient-contact, insulated, electrical cord with a connector (plug) at both ends designed to transmit electrical power and/or signal (data) between medical devices (e.g., to connect a lead, electrical catheter, handpiece, or monitor to a parent device). It is not intended to connect directly to patient-worn electrodes (i.e., it is not a lead), is not intended to connect to the mains (i.e., not a mains power cable), does not generate any type of power and/or signal, and has no additional non-electrical conducting or processing functionality. This is a reusable device.


Environmental Conditions

  • Handling Environment Temperature - Degrees Celsius
    • 70.00
    • -40.00
  • Storage Environment Humidity - Percent (%) Relative Humidity
    • 95.00
    • N/A
  • Storage Environment Temperature - Degrees Celsius
    • 30.00
    • 15.00

  • Device Sizes

  • Length: 1.83 Meter
    • Length: 1.83 Meter


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: True

    Sterilization Methods:

  • Ethylene Oxide
  • Moist Heat or Steam Sterilization
    • Ethylene Oxide
    • Moist Heat or Steam Sterilization


    Product Codes

    Code: LWP

    Device Name: Implantable Pulse Generator, Pacemaker (Non-Crt)

    Device Class: 3

    Physical State: These devices treat bradycardia (slow heartbeats) with RA and/or RV pacing therapy as necessary.

    Definition: These devices treat bradycardia (slow heartbeats) with RA and/or RV pacing therapy as necessary.

    Submission Type ID: 2

    Review Panel: CV

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: These devices treat bradycardia (slow heartbeats) with RA and/or RV pacing therapy as necessary.

    Life Sustain Support Flag: Y

    Unclassified Reason: N/A

    Implant Flag: Y

    Target Area: These devices treat bradycardia (slow heartbeats) with RA and/or RV pacing therapy as necessary.

    Regulation Number: N/A

    Third Party Flag: N

    Medical Specialty: N/A


    Device Identifiers

    Device Id: 00763000181208

    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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