SNARE GN2000 GOOSENECK SNARE V02


Product Overview

SNARE GN2000 GOOSENECK SNARE V02
Amplatz Goose Neck™ - GN2000


Device Description

A flexible, end- and/or side-hole tube with a long snaring device (e.g., a wire loop or noose) inserted through its lumen, designed to be introduced into a blood vessel or similar structure to manually retrieve or manipulate a foreign body. It is typically available in two forms: 1) the loop emerges from the distal tip of the catheter while both free ends of the wire emerge from the proximal end; and 2) the end of the wire is attached to the distal end of the catheter while the free end is passed through the lumen to emerge at the proximal end. The wire is usually made of a high-strength, stiff metal [e.g., nickel-titanium alloy (Nitinol)].


Environmental Conditions

  • Special Storage Condition, Specify
    • Keep away from sunlight
  • Special Storage Condition, Specify
    • Keep dry

  • Device Sizes

  • Snare length 120 cm
  • Catheter tip OD 6.5 FR
  • Catheter Gauge: 6.1 French
  • Loop diameter 20 mm
  • Catheter Working Length: 102.0 Centimeter
  • Catheter Inner Diameter: 1.6 Millimeter
  • Wire diameter 1.32 mm
    • Snare length 120 cm
    • Catheter tip OD 6.5 FR
    • Catheter Gauge: 6.1 French
    • Loop diameter 20 mm
    • Catheter Working Length: 102.0 Centimeter
    • Catheter Inner Diameter: 1.6 Millimeter
    • Wire diameter 1.32 mm


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: DXE

    Device Name: Catheter, Embolectomy

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: CV

    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: 870.5150

    Third Party Flag: Y

    Medical Specialty: CV


    Code: MMX

    Device Name: Device, Percutaneous Retrieval

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: CV

    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: 870.5150

    Third Party Flag: Y

    Medical Specialty: CV


    Device Identifiers

    Device Id: 00763000762391

    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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