BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    ANGIODYNAMICS, INC. 600UM FIBER AND VENACURE PROCEDURE KIT

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

    Cordant

    FDA UDI
    Seaspine Orthopedics Corporation·10889981115371·78mm

    TRIO LX SMALL CONNECTOR

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code MNI·March 23, 2011

    HEDROCEL VERTEBRAL BODY REPLACEMENT, MODEL XX-YYY-ZZZZ

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BACT/ALERT MB CULTURE BOTTLE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·April 22, 2013

    ACCU-CHEK FLEXLINK PLUS

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code FRN·April 18, 2011

    ALLEZ SPINE LAGUNA PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Malfunction ·ALLEZ SPINE, LLC·Product code MNI·July 3, 2008

    CT EXPRES

    FDA Adverse Event
    Injury ·BRACCO INJENEERING S.A.·Product code IZQ·September 27, 2023