BEUDAMED
    7,559 results · 22ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·HER OPTION OFFICE CRYOABLATION THERAPY SYSTEM

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·Mara Water Vapor System

    Fluid, Hysteroscopy

    FDA Pre-Market Approval
    FDA Class 3 ·HYSKON (32% DEXTRAN 70)

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·HER OPTION CRYOABLATION THERAPY SYSTEM

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·AEGEA Water Vapor Ablation System

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·HER OPTION CRYOABLATION THERAPY SYSTEM

    Device, Thermal Ablation, Endometrial

    FDA Pre-Market Approval
    FDA Class 3 ·Mara Vapor System

    Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes

    FDA classification
    FDA Class 3 ·Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes

    Permanent Defibrillator Electrodes

    FDA classification
    FDA Class 3 ·Permanent Defibrillator Electrodes

    STYLET INTRODUCER FUNNEL

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    QMPLANTABLE PROGRAM. CARDIAC PULSE GEN. W/TELEMETR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    IMPLANTABLE ELECTRODE LEAD 030-271 USING POLYURETH

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    IMPLANTABLE PROGRAMMABLE CARDIAC PULSE GENERATORS

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    IMPLANTABLE ELECTRODE ADAPTOR ASSEMBLE

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    IMPLANTABLE ELECTRODE LEAD, MODEL 030-400

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    MODEL 1740 PERSONAL POCKET PROGRAMMER

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    DDU-120 FULLY AUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    RESUBMISSION OF MODEL 030-437 IMPLANT. ELECTRODE

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    IMPLANT PROGRAM CARDIAC PULSE GEN W/MOD SET SCREW

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    DEFIBTECH AED WITH ATTENUATED DEFIBRILLATION/MONITORING PADS, MODELS DDU-100 WITH DDP-200P

    FDA 510(k)
    FDA Class 3 ·Cardiovascular