BEUDAMED
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    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·LORDOTEC(TM) TAPERED FUSION DEVICE

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK VISTA INTERBODY FUSION CAGE

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODELS 940 & 941 VISTA DDD GEN. & MODEL 2050 MODUL

    FLEX Mono Mo A-Hu CD23 Cl DAK-CD23 RTU

    FDA UDI
    AGILENT TECHNOLOGIES SINGAPORE PTE LTD·05700572032588·FLEX Monoclonal Mouse Anti-Human CD23 Clone DAK...

    FLEX Mono Mo A-Hu CDX2 Cl DAK-CDX2 RTU

    FDA UDI
    AGILENT TECHNOLOGIES, INC.·05700571101407·FLEX Monoclonal Mouse Anti-Human CDX2 Clone DA...

    Schlauchsystem mit Konus Gr. 1 DK

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Schaefers Medizintechnik GmbH·1 device

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·RAY TFC DEVICE AND RAY TFC UNITE DEVICE

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BRANTIGEN I/F CAGE(R) USED WITH VSP(R) SPINE PLATES AND PEDICLE SCREWS

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·BAK VISTA INTERBODY FUSION CAGE

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA Pre-Market Approval
    FDA Class 2 ·DUAL INTERFIX-RP(TM) THREADED FUSION DEVICE

    Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 446 & 447 VISTA T,MODEL 940 & 941 VISTA DDD

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 446 & 447 VISTA T,MODEL 940 & 941 VISTA DDD

    K-ASSAY HS-CRP CONTROLS

    FDA 510(k)
    FDA Class 2 ·Immunology

    ANTISERUM TO HUMAN, ALPHA-2-MACROGLOBULI

    FDA 510(k)
    FDA Class 2 ·Immunology

    SPQ TEST SYSTEM FOR C-REACTIVE PROTEIN

    FDA 510(k)
    FDA Class 2 ·Immunology

    CIC-C1Q EIA

    FDA 510(k)
    FDA Class 2 ·Immunology

    HUMAN C-REACTIVE PROTEIN KIT (MODIFICATION)

    FDA 510(k)
    FDA Class 2 ·Immunology

    LAS-R HUMAN COMPLEMENT CLQ TEST

    FDA 510(k)
    FDA Class 2 ·Immunology