BEUDAMED
    86 results · 22ms · Sources: EU EUDAMED, US FDA

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    AFGHAN EXTERNAL FIXATOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PureLife+ 2-Ply Dental Bibs

    FDA UDI
    PURELIFE, LLC·D79010920021·PureLife+ 2-Ply Dental Bibs, Pink, 2-ply paper,...

    NuOss XC Socket

    FDA UDI
    COLLAGEN MATRIX, INC.·00813954027982·Self-Expanding Composite

    NuOss

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950009480·NUOSS XC SOCKET 9X15MM SYRINGE

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065647·INTRAORAL ELASTICS 2,5 oz 3/16" green

    Ocata Anterior Cervical System

    FDA UDI
    Kalitec Direct LLC·B07308K0120020·Driver Shaft, Final Tighten

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0120020·T-Handle, T25, Screw Height Adjuster

    SUREFIT DISPERSIVE ELECTRODE

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

    VIKING OPTIMA GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CLARION

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS CORPORATION·Product code MCM·October 22, 2002

    QUICK SET

    FDA Adverse Event
    Malfunction ·MAERSK MEDICAL A/S·Product code FPA·September 16, 2002

    H-TRONPLUS

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code LZG·January 3, 2005

    QUICK SET

    FDA Adverse Event
    Malfunction ·MAERSK MEDICAL DEVICES SADECV·Product code FPA·September 19, 2002

    NCP PULSE GENERATOR

    FDA Adverse Event
    Death ·CYBERONICS, INC.·Product code LYJ·October 30, 2002

    QUICK SET

    FDA Adverse Event
    Malfunction ·MAERSK MEDICAL DEVICES SADECV·Product code FPA·September 19, 2002

    QUICK SET

    FDA Adverse Event
    Malfunction ·MAERSK MEDICAL DEVICE SADECV·Product code FPA·September 19, 2002

    AMICUS APHERESIS KIT - CLSD SGL NDL

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORP.·Product code GKT·October 25, 2002

    SERIES TEN THOUSAND OCUTOME

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQE·September 25, 2002

    SILHOUETTE

    FDA Adverse Event
    Malfunction ·MAERSK MEDICAL A/S·Product code FPA·December 17, 2002

    HYDROVIEW INTRAOCCULAR LENS

    FDA Adverse Event
    Injury ·BAUSCH & LOMB·Product code HQL·December 5, 2002