BEUDAMED
    2,623 results · 40ms · Sources: EU EUDAMED, US FDA

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Filler, Bone Void, Synthetic Peptide

    FDA Pre-Market Approval
    FDA Class 3 ·PearlMatrix™ Bone Graft

    Test, Volatile Organic Compounds Breath Analysis

    FDA classification
    Test, Volatile Organic Compounds Breath Analysis

    Dvd, Bluray, Or Hd Recorder

    FDA classification
    FDA Not Classified ·Dvd, Bluray, Or Hd Recorder

    HD 60144656

    Certificate
    MDD Annex II (excluding section 4)·Substrate HD·TÜV Rheinland LGA Products GmbH·1 Basic UDI-DI

    Acute Coronary Syndrome Event Detector

    FDA Pre-Market Approval
    FDA Class 3 ·Guardian System

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    DUP9340 Gazetex 100% Cotton , 6-ply, Fluff Sponge 6" x 6I-3/4" Sterile

    FDA registration
    DERMA SCIENCES NANTONG INCORPORATION·1 product·🇨🇳 China

    DUP9340 Gazetex 100% Cotton , 6-ply, Fluff Sponge 6" x 6I-3/4" Sterile

    FDA registration
    DERMA SCIENCES CANADA, INC (dba DERMA SCIENCES, INC.)·1 product·🇨🇦 Canada

    Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus

    FDA Pre-Market Approval
    FDA Class 2 ·HOME ACCESS HEPATITIS C CHECK

    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

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·ADVISA SR MRI

    Dorsal Root Ganglion Stimulator For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·Axium Neurostimulator System

    MED-RAS GmbH Regulatory Affairs Service

    Authorized representative
    🇩🇪 Germany·18 Manufacturers·235 Devices

    Dvd, Dvd-Rom, Bluray, Hd Player

    FDA classification
    FDA Not Classified ·Dvd, Dvd-Rom, Bluray, Hd Player

    Acute Coronary Syndrome Event Detector

    FDA Pre-Market Approval
    FDA Class 3 ·AngelMed Guardian System

    Implantable Pulse Generator, Pacemaker (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·VITALITY DS ICD SYSTEMS

    Portex

    FDA UDI
    Smiths Medical International Ltd·10351688433954·