BEUDAMED
    377 results · 20ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Replacement Heart-Valve

    FDA Pre-Market Approval
    FDA Class 3 ·CARPENTIER-EDWARDS DURAFLEX LOW PRESSURE BIOPROSTHESIS

    Replacement Heart-Valve

    FDA Pre-Market Approval
    FDA Class 3 ·CARPENTIER-EDWARDS DURAFLEX LOW PRESSURE BIOPROSTHESIS

    Replacement Heart-Valve

    FDA Pre-Market Approval
    FDA Class 3 ·CARPENTIER-EDWARDS DURAFLEX LOW PRESSURE MITRAL

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

    FDA Pre-Market Approval
    FDA Class 3 ·Isoflex Low Voltage Passive Fixation Leads

    Replacement Heart-Valve

    FDA Pre-Market Approval
    FDA Class 3 ·HANCOCK LOW POROSITY CONDUIT MODEL 105

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·TENDRIL FAMILY F LOW VOLTAGE LEADS

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

    FDA Pre-Market Approval
    FDA Class 3 ·Tendril and OptiSense Low Voltage Leads

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·Precision Spinal Cord Stimulator Systems

    Stimulator, Electrical, Implanted, For Parkinsonian Symptoms

    FDA Pre-Market Approval
    FDA Class 3 ·Vercise Deep Brain Stimulation Systems

    Stimulator, Autonomic Nerve, Implanted For Epilepsy

    FDA Pre-Market Approval
    FDA Class 3 ·SenTiva Model 1000 and SenTiva Duo Model 1000-D 2024 Generator Firmware Maintenance

    Device, Testicular Hypothermia

    FDA Pre-Market Approval
    FDA Class 3 ·REPRO-MED - THD

    Device, Testicular Hypothermia

    FDA Pre-Market Approval
    FDA Class 3 ·REPRO-MED - THD ADDRESS CHANGE / MANU. FACILITY

    Device, Testicular Hypothermia

    FDA Pre-Market Approval
    FDA Class 3 ·REPRO-MED - THD

    Device, Testicular Hypothermia

    FDA Pre-Market Approval
    FDA Class 3 ·REPRO-MED - THD

    Device, Testicular Hypothermia

    FDA Pre-Market Approval
    FDA Class 3 ·REPRO-MED - THD

    Device, Testicular Hypothermia

    FDA Pre-Market Approval
    FDA Class 3 ·REPRO-MED - THD

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·COLLAGRAFT STRIP BONE GRAFT MATRIX

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·COLLAGRAFT(TM) BONE GRAFT SUBSTITUTE

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·COLLAGRAFT(TM) BONE GRAFT MATRIX

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·COLLAGRAFT(TM) BONE GRAFT MATRIX