The Acessa ProVu Handpiece is an RF ablation device to be connected to the Acessa ProVu System. The Acessa ProVu Handpiece is designed to function with or without tracking. The Acessa ProVu Handpiece is equipped with a slider knob to control the deployment and retraction of the needle array.


Product Overview

The Acessa ProVu Handpiece is an RF ablation device to be connected to the Acessa ProVu System. The Acessa ProVu Handpiece is designed to function with or without tracking. The Acessa ProVu Handpiece is equipped with a slider knob to control the deployment and retraction of the needle array.
Acessa ProVu System - 7300


Device Description

An electrosurgical device consisting of a handpiece with mechanical and/or electrical controls, and a monopolar electrode, intended to deliver a current from a system generator directly to tissues for cutting/coagulation/ablation during endoscopic (including laparoscopic, arthroscopic) surgery. It includes a long thin electrode connected to the handpiece and requires a patient contact return electrode; it may include a suction/irrigation lumen and may feature a magnetic guidance sensor for electromagnetic tracking. It is available in a variety of forms (e.g., forceps or snare with ring handles, rigid probe) and may also be designed to mechanically cut tissues. This is a single-use device.


Environmental Conditions

  • Handling Environment Temperature - Degrees Celsius
    • 30.00
    • 10.00
  • Storage Environment Temperature - Degrees Celsius
    • 65.00
    • -34.00

  • Device Sizes

    No Data Available


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: HFG

    Device Name: Coagulator, Laparoscopic, Unipolar (And Accessories)

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: OB

    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: 884.4160

    Third Party Flag: Y

    Medical Specialty: OB


    Device Identifiers

    Device Id: 15420045515246

    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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