BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    Bi-Flex Evo

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Bernafon

    FDA UDI
    Bernafon AG·05711584078709·AQ CO9 MNR T, 2.4G NFM DPB COBR ACCUQ

    PROPELLER HEAD SCREW SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304269521·

    Larger Tapered Pin Reamer

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215055615·

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·October 18, 2002

    AEQUALIS SHOULDER FRACTURE SYSTEM, AEQUALIS REVERSED SHOULDER PROSTHESIS, AEQUALIS REVERSED FRACTURE SHOULDER PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AMICAS PACS, VERSION 6.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, NEUROMODULATION·Product code LGW·June 14, 2013

    DAMON COPPER NITI WIRE

    FDA Adverse Event
    Malfunction ·ORMCO CORPORATION·Product code DZC·October 2, 2008

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·June 23, 2011

    ENDURANT STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·March 26, 2019