Kidney Shape Balloon


Product Overview

Kidney Shape Balloon
PDB - OMS-PDBS2


Device Description

A device designed to dissect connective tissue layers creating access to a desired surgical site during a laparoscopic procedure. It typically consists of a cannula, a distention balloon, an obturator, an inflation bulb, and a regulating valve(s). An appropriate endoscope is introduced into the cannula to monitor the dissection and/or the insertion process. Using the inflation bulb, the balloon is inflated to a recommended fill volume exerting pressure on the tissue layers. Once the space is dissected the balloon is deflated and the device replaced by other suitable devices (e.g., trocar/cannula) whilst the peritoneal space is insufflated under low pressure. This is a single-use device.


Environmental Conditions

  • Handling Environment Temperature - Degrees Fahrenheit
    • 130.00
    • N/A

  • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: GEX

    Device Name: Powered Laser Surgical Instrument

    Device Class: 2

    Physical State: N/A

    Definition: A laser (light amplification by stimulated emission of radiation) based device having coherence, collimated and typically monochromatic radiation. Typically indicated to to cut, destroy, remove or coagulate tissue, generally soft tissue, for general surgical purpose in medical specialties of general and plastic surgery, dermatology/aesthetic, podiatry, otolaryngology (ent), gynecology, neurosurgery, orthopedics (soft tissue), dental and oral surgery, and dentistry. The classification regulation 21 cfr 878.4810 describes a device that is carbon dioxide or argon laser intended to cut, destroy, remove or coagulate tissue by the light.

    Submission Type ID: 1

    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: 878.4810

    Third Party Flag: Y

    Medical Specialty: SU


    Device Identifiers

    Device Id: 20884521067940

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 10884521067943

    Package Quantity: 5

    Package Discontinue Date: N/A

    Package Status: In Commercial Distribution

    Package Type: CASE


    Device Id: 10884521067943

    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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