Side-Port Syringe


Product Overview

Side
Aliquot - 2110-0513


Device Description

A collection of sterile surgical instruments, tools, and materials designed to prepare and apply bone cement during an orthopaedic surgical procedure (e.g., hip replacement, arthroplasty, or vertebroplasty). It typically includes items such as forceps, a mallet, cement delivery injectors, delivery tubes, and mixing devices; it may or may not include bone cement. This is a single-use device.


Environmental Conditions

  • Storage Environment Temperature - Degrees Celsius
    • 30.00
    • 20.00

  • Device Sizes

  • Total Volume: 1.0 Cubic Centimeter
    • Total Volume: 1.0 Cubic Centimeter


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: OAR

    Device Name: Injector, Vertebroplasty (Does Not Contain Cement)

    Device Class: 1

    Physical State: plastic syringe type device -- some embodiments may include levers or screws to increase injection force or control

    Definition: Intended for injection of vertebroplasty bone cement for the fixation of pathological fractures of the vertebral body using vertebroplasty or kyphoplasty procedures. Painful vertebral compression fractures may result from osteoporosis, benign lesions (hemangioma), and malignant lesions (metastatic cancers, myeloma).

    Submission Type ID: 4

    Review Panel: OR

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: Uses mechanical force to inject bone cement into vertebra

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: vertebra

    Regulation Number: 888.4200

    Third Party Flag: N

    Medical Specialty: OR


    Code: KIH

    Device Name: Dispenser, Cement

    Device Class: 1

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 4

    Review Panel: OR

    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: 888.4200

    Third Party Flag: N

    Medical Specialty: OR


    Device Identifiers

    Device Id: 00808232001150

    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


    GMDN ®. © GMDN Agency 2005-2024.
    Educational Resources
    Videos