Penrose Drain 12" (304.8mm), X-Ray Opaque Rubber, 5/8" (15.88mm)


Product Overview

Penrose Drain 12" (304.8mm), X
Penrose Drain - 0912040


Device Description

A sterile device with a lumen(s) designed to establish a passive egress for the removal of fluid (drainage of blood, lymph, exudate) from a surgical wound to minimize its accumulation and risk of wound infection; it is not dedicated to a particular anatomical wound. It is typically inserted into the wound by a surgeon in the operating room (OR) after the completion of an inpatient or outpatient procedure. It is made of radiopaque Hevea natural rubber latex (NRL) and is available in various forms (e.g., Penrose type). This is a single-use device.


Environmental Conditions

  • Special Storage Condition, Specify
    • Keep away from sunlight

  • Device Sizes

  • Length: 12 Inch
    • Length: 12 Inch


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: GBX

    Device Name: Catheter, Irrigation

    Device Class: 1

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 4

    Review Panel: SU

    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: 878.4200

    Third Party Flag: N

    Medical Specialty: SU


    Device Identifiers

    Device Id: 20801741051269

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 10801741051262

    Package Quantity: 4

    Package Discontinue Date: N/A

    Package Status: In Commercial Distribution

    Package Type: CA


    Device Id: 10801741051262

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 00801741051265

    Package Quantity: 50

    Package Discontinue Date: N/A

    Package Status: In Commercial Distribution

    Package Type: BX


    Device Id: 00801741051265

    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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