CONNECTOR 6107 3/8 Y LL


Product Overview

CONNECTOR 6107 3/8 Y LL
Intersept® - 6107


Device Description

A collection of sterile devices including tubing and typically clamps, filters, connectors, and stopcocks, used in a circuit for a cardiopulmonary bypass procedure. The tubing is typically polymeric and may be heparin coated. It is typically used in the blood pump head of a cardiopulmonary bypass system. The tubing, when used in a roller type pump, will be cyclically compressed by the blood pump to cause the blood to flow through the heart-lung bypass system. This is a single-use device.


Environmental Conditions

No Data Available


Device Sizes

  • 9.5 MM Port Outer Diameter
    • 9.5 MM Port Outer Diameter


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: True

    Sterilization Methods:

  • Ethylene Oxide
    • Ethylene Oxide


    Product Codes

    Code: DTL

    Device Name: Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 4

    Review Panel: CV

    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: 870.4290

    Third Party Flag: N

    Medical Specialty: CV


    Code: DWE

    Device Name: Tubing, Pump, Cardiopulmonary Bypass

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: CV

    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: 870.4390

    Third Party Flag: Y

    Medical Specialty: CV


    Device Identifiers

    Device Id: 20673978555151

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 00673978555157

    Package Quantity: 20

    Package Discontinue Date: 5/2/2019 12:00:00 AM

    Package Status: Not in Commercial Distribution

    Package Type: PK


    Device Id: 00673978555157

    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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