BEUDAMED
    11 results · 34ms · Sources: EU EUDAMED, US FDA

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    EXMOOR AURAL GROMMET AG/T2

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    OTS PG&E Field Kit

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588107035·OTS PG&E Field Kit

    INTER-VIAL

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD AUTOSHIELD DUO PEN NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD INSULIN PEN NEEDLE

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code FMI·November 9, 2015

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 9, 2014

    CAPSURE SP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    1644487-2008-00539

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·February 29, 2008

    STANDARD INSERTION HANDLE

    FDA Adverse Event
    Injury ·SYNTHES HAGENDORF·Product code LXH·July 14, 2017

    PERIARTICULAR AIMING ARM FOR 4.5MM LCP CURVD CONDYLAR PL-LT

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code FZX·July 14, 2017

    GALAXY G3 MINI 2MM X 6CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·July 29, 2021