BEUDAMED
    374 results · 18ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·TENDRIL SDX PERMANENT PACEMAKER LEADS, MODELS 1688T/TC

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC{R} CAPSURE{TM} MODEL 5052/5525

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 5023M UNIPOLAR PACING LEAD

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·FINELINE FAMILY INCLUDES FINELINE, FINELINE II

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSURE SP NOVUS/Z NOVUS

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·CARBON TIPPED LEAD MODELS 1085S,1085M,& 1085K

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·FLEXTEND LEADS, MODELS 4086, 4087, AND 4088

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·SELUTE,SELUTE PICOTIP

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·THIN LINE AND FINELINE PACING LEADS

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSURE(R) AND CAPSURE(R)SP LEADS

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC CAPSURE(R) SP MODEL 5024M/5524M PACING LEADS

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC(R) CAPSURE(R) EPI PACING LEAD MODEL 4695

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSURE SP/SENSE/SP NOVUS

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·PHILOS PACING SYSTEM

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·PHILOS DR-T PULSE GENERATOR

    Immunohistochemistry Assay, Antibody, Programmed Death-Ligand 1

    FDA Pre-Market Approval
    FDA Class 3 ·VENTANA PD-L1(SP142) CDX ASSAY

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Pipeline™ Flex Embolization Device (Pipeline™ Flex); Pipeline™ Flex Embolization Device with Shield Technology™ (Pipelin

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·PIPLINE TM EMBOLIZATION DEVICE

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Pipeline Flex Embolization Device

    Intracranial Aneurysm Flow Diverter

    FDA Pre-Market Approval
    FDA Class 3 ·Pipeline™ Vantage Embolization Device with Shield Technology™ (Pipeline™ Vantage)