BEUDAMED
    36 results · 30ms · Sources: EU EUDAMED, US FDA

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    THE FUGO BLADE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Custom Procedure Kit

    FDA UDI
    MEDIVATORS INC.·40677964014664·The ENDO CARRY-ON Procedure Kit contains all of...

    GRADIA®

    FDA UDI
    Gc America Inc.·D0470014981·GRADIA® INTENSIVE COLOR IC2

    GRADIA®

    FDA UDI
    Gc America Inc.·14548161392891·GRADIA® INTENSIVE COLOR IC2

    RMO

    FDA UDI
    Rmo, Inc.·00885797099686·MAX MLR BDS ASST 100 SE ASIA

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001498·artVeneer life upper anteriors, BXL, D4

    COHERENT LASERLINK Z-1000 SLIT LAMP LASER DELIVERY ADAPTER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PRO.DUCT HEALTH MICRO-STYLET, MODEL STY01

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GLADIATOR® G26 BIPOLAR

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LZO·August 30, 2024

    BD Q-SYTE LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·August 18, 2020

    PTERYFIT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·October 22, 2025

    PTERYFIT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·December 17, 2025

    PTERYFIT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·October 20, 2025

    EON

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 5, 2013

    CAROTID WALLSTENT MONORAIL ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIM·February 25, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·February 19, 2008

    BD Q-SYTE CLOSED LUER ACCESS DEVICE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FPA·August 28, 2024

    BD Q-SYTE LUER ACCESS SPLIT SEPTUM

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·June 22, 2022

    BD Q-SYTE CLOSED LUER ACCESS DEVICE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FPA·September 16, 2024

    BD Q-SYTE CLOSED LUER ACCESS DEVICE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FPA·September 4, 2024