BEUDAMED
    3,717 results · 42ms · Sources: EU EUDAMED, US FDA

    Monoart

    FDA UDI
    EURONDA SPA·E3072902061·Practical kit Monoart containing 5 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E30729017110·Practical kit Monoart containing 4 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E3072902101·Practical kit Monoart containing 5 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E30729020710·Practical kit Monoart containing 5 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E30729017817·Practical kit Monoart containing 4 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E3072902011·Practical kit Monoart containing 5 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E3072903501·Practical kit Monoart containing 4 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E3072902051·Practical kit Monoart containing 5 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E30729020811·Practical kit Monoart containing 5 different di...

    Monoart

    FDA UDI
    EURONDA SPA·E3072902031·Practical kit Monoart containing 5 different di...

    Injectate Kit, EUW

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·LiDCO Ltd·1 device

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·BELOS, LEXOS, LUMOS, and XELOS

    Implantable Pacemaker Pulse-Generator

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 1802.U, ACTROS, AXOS, BA03, CYLOS, DROMOS, KAIROS, PHILOS, PHILOS II, PROTOS, EVIA, ENTOVIS, ECURO, EFFECTA, ESTELLA

    Pacemaker/Icd/Crt Non-Implanted Components

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2201.U/1 and NEO 2201.U/1

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·IFORIA 5/7, ILESTO 57/, INVENTRA 7, IPERIA 5/7, ITREVIA 5/7, ILIVIA 5/7, INTICA 5/7, INLEXA 5/7, LUMAX 300/340 and 500/5

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2201.U/1 and NEO 2201.U/1

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2201.U/1 and NEO 2201.U/1

    Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

    FDA Pre-Market Approval
    FDA Class 3 ·STRATOS, EVIA, ENTOIVS, ELUNA 8, EPYRA 8, and ETRINSA 8

    Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2201.U/1 and NEO 2201.U/1

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·PSW 2201.U/1 and NEO 2201.U/1