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Results for “Guide Device”

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677 devices foundsorted by relevance

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  • Torque Device for Guidewire MZCH-2-12

    Amsinomed Medical Co., Ltd,FDA registration: United States
    None Registry: GUDID Class:I

  • Worker™ Guidewire 120135180

    Argon Medical Devices, Inc.,United States
    Withdrawn Registry: GUDID Class:II

  • Guidewire 395863

    Argon Medical Devices, Inc.,United States
    Withdrawn Registry: GUDID Class:II

  • Guidewire 395835

    Argon Medical Devices, Inc.,United States
    Withdrawn Registry: GUDID Class:II

  • Guidewire 395258

    Argon Medical Devices, Inc.,United States
    Withdrawn Registry: GUDID Class:II

  • Orientable Alignment Guide - Supine 20°/45° AAZ011-000

    Incipio Devices,FDA registration: United States
    Active Regimes: CE MDR Registry: GUDID Class:I

  • WORKER™ Guidewire 126035180

    Argon Medical Devices, Inc.,United States
    Withdrawn Registry: GUDID Class:II

  • Guidewire 395692

    Argon Medical Devices, Inc.,United States
    Withdrawn Registry: GUDID Class:II

  • Polyaxial Drill Guider Retainer MDS14120701

    Miami Device Solutions,FDA registration: United States
    None Registry: GUDID Class:II

  • Guidewire 395874

    Argon Medical Devices, Inc.,United States
    Withdrawn Registry: GUDID Class:II

  • Guidewire 395278

    Argon Medical Devices, Inc.,United States
    Withdrawn Registry: GUDID Class:II

  • Guidewire 395213

    Argon Medical Devices, Inc.,United States
    Withdrawn Registry: GUDID Class:II

  • Guidewire 395839

    Argon Medical Devices, Inc.,United States
    None Registry: GUDID Class:II

  • Freehand Drill Guide MDS190812

    Miami Device Solutions,FDA registration: United States
    None Registry: GUDID Class:II

  • Polyaxial Drill Guide Retainer, 2.7T MDS10120701

    Miami Device Solutions,FDA registration: United States
    None Registry: GUDID Class:II

  • Polyaxial Drill Guide Screw MDS110802

    Miami Device Solutions,FDA registration: United States
    None Registry: GUDID Class:II

  • Polyaxial Drill Guide Sleeve MDS110803

    Miami Device Solutions,FDA registration: United States
    None Registry: GUDID Class:II

  • Guidewire 395398

    Argon Medical Devices, Inc.,United States
    Withdrawn Registry: GUDID Class:II

  • Guidewire 395844

    Argon Medical Devices, Inc.,United States
    Withdrawn Registry: GUDID Class:II

  • Guidewire 395268

    Argon Medical Devices, Inc.,United States
    Withdrawn Registry: GUDID Class:II

Showing 401-420 of 677