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

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    PROGENIX PLUS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Cook

    FDA UDI
    COOK INCORPORATED·00827002142275·Percutaneous Nephrostomy Accessory Set

    FIBONACCI™ PROXIMAL LATERAL TIBIA PLATE, RIGHT, 2 HOLE

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665035230·

    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

    NCP BIPOLAR LEAD

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·June 28, 2002

    TOTAL CARE

    FDA Adverse Event
    Other ·HILL-ROM RITTER·Product code FNL·August 8, 2002

    QUICK SET MARILYN

    FDA Adverse Event
    Malfunction ·MAERSK MEDICAL DEV. S.A. DE C.V.·Product code FPA·January 15, 2003

    TOTAL CARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 23, 2002

    ACCURUS 600DS

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQE·February 7, 2002

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·August 19, 2002

    PERI-STRIPS DRY

    FDA Adverse Event
    Death ·SYNOVIS SURGICAL INNOVATIONS·Product code FTL·September 16, 2002

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code LKK·March 6, 2003

    MEDISYSTEMS

    FDA Adverse Event
    Death ·MEDISYSTEMS CORPORATION·Product code FJK·September 20, 2002

    ONE TOUCH II

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·August 21, 2002

    ONE TOUCH BASIC

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·August 21, 2002

    LADARVISION EXCIMER LASER SYSTEM

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code LZS·August 16, 2002

    EAR WASH SYSTEM PLUS

    FDA Adverse Event
    Injury ·WELCH ALLYN·Product code KYZ·October 22, 2004