Monoplane Interventional X-Ray System. A ceiling monoplane system with a 12-inch flat detector.


Product Overview

Monoplane Interventional X
Azurion - Azurion 5 M12


Device Description

A stationary diagnostic fluoroscopic x-ray system specifically designed to optimize the capability of users to visually and quantitatively evaluate the anatomy and function of blood vessels of the heart, brain and other organs, as well as the lymphatic system. It uses digital techniques for real-time image capture, display and manipulation and typically includes spot-film capabilities in addition to the fluoroscopic features. It is commonly used in conjunction with an injected x-ray contrast medium during either imaging or x-ray guided surgical or interventional procedures. Images can be viewed in both real-time and delayed formats.


Environmental Conditions

  • Storage Environment Atmospheric Pressure - KiloPascal
    • 110.00
    • 70.00
  • Storage Environment Humidity - Percent (%) Relative Humidity
    • 95.00
    • 5.00
  • Storage Environment Temperature - Degrees Fahrenheit
    • 158.00
    • -13.00
  • Storage Environment Temperature - Degrees Celsius
    • 70.00
    • -25.00

  • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: OWB

    Device Name: Interventional Fluoroscopic X-Ray System

    Device Class: 2

    Physical State: Fluoroscopic X-Ray system

    Definition: Interventional fluoroscopy

    Submission Type ID: 1

    Review Panel: RA

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: Fluoroscopy

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: Human body

    Regulation Number: 892.1650

    Third Party Flag: Y

    Medical Specialty: RA


    Code: JAA

    Device Name: System, X-Ray, Fluoroscopic, Image-Intensified

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: RA

    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: 892.1650

    Third Party Flag: Y

    Medical Specialty: RA


    Device Identifiers

    Device Id: 00884838116740

    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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