BEUDAMED
    585 results · 17ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·PASSIVE PLUS DX, MODELS 1336T, 1342T, 1343K, 1345K, 1346T

    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

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·CLARITY /VITATRON DA+ C-SERIES/DIAMOND 3/JADE 3/RUBY 3/VITATRON DA+ T-SERIES/TOPAZ 3/VITA 2/VITA IPGS

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·CLARITY/VITATRON DA+C-SERIES/DIAMOND 3/JADE 3/RUBY 3/VITATRON DA+T-SERIES/TOPAZ 3/VITA 2/VITA IPGS

    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