HD Laparoscope, Autoclavable, 0 ¿ View Direction


Product Overview

HD Laparoscope, Autoclavable, 0 ¿ View Direction
AIM (Advanced Imaging Modality) - 0502537010


Device Description

An endoscope with a rigid inserted portionangulus iridocornealis for the visual examination and treatment of the abdominal/retroperitoneal cavity and its organs. It is inserted through an incision made in the abdominal wall (routinely just below the umbilicus) during laparoscopy. Anatomical images are transmitted to the user by the device through relayed lens optics or a fibreoptic bundle. The abdominal wall is distended, typically using a gas, providing the space to allow the surgeon to view and/or operate on the exposed organs. This reusable device is commonly used to evaluate/treat abdominal or pelvic pain, ectopic pregnancy, ovarian cysts, appendicitis, and perform female sterilization.


Environmental Conditions

No Data Available


Device Sizes

  • Length: 30.0 Centimeter
  • Outer Diameter: 5.4 Millimeter
    • Length: 30.0 Centimeter
    • Outer Diameter: 5.4 Millimeter


    Device Sterilization

    Device Sterile: False

    Sterilization Prior To Use: True

    Sterilization Methods:

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


    Product Codes

    Code: OWN

    Device Name: Confocal Optical Imaging

    Device Class: 2

    Physical State: Usually include optical fibers, light collection cameras and computer-based central processing unit

    Definition: Collection of light signals for visualization of cellular microstructures.

    Submission Type ID: 1

    Review Panel: SU

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: Collects reflected and scattered light signals from the areas of interest for image reconstruction

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: soft tissue, blood vessel and other vessels in the body

    Regulation Number: 876.1500

    Third Party Flag: N

    Medical Specialty: GU


    Device Identifiers

    Device Id: 07613327059342

    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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