BEUDAMED
    11 results · 26ms · Sources: EU EUDAMED, US FDA

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    ENDOSEE MODEL 8000 U-SCOPE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    NA

    FDA UDI
    GENDRON, INC.·00842307101079·STRETCHER,CHR FRM,ENAM LTR

    IFS LASER SYSTEM

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

    NEBULAE I

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 13, 2017

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·October 15, 2025

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·May 21, 2013

    RESTORE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·September 26, 2014

    IMPLANTIUM

    FDA Adverse Event
    Injury ·DENTIUM USA·Product code DZE·June 9, 2011

    TOSOH ST AIA 25-OH VITAMIN D PRETREATMENT SET

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code MRG·April 19, 2018