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

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    Arthrex Mesh Plates

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DJO SURGICAL

    FDA UDI
    Encore Medical, L.P.·00190446840916·SPECIAL, ALTIVATE REVERSE HUMERAL BROACH, 8 X 1...

    HHM

    FDA UDI
    Oticon A/S·05707131357175·G500 SC, MINIRITE R LI-ION 2.4G C063 HHM

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116023141·DMTL SmartFlex 200 High Energy Reusable (5X)

    CODMAN

    FDA UDI
    Cerenovus, Inc.·10886704001591·CODMAN SLIM-LINE Aneurysm Clip Super Bayonet Bl...

    NA

    FDA UDI
    Synthes GmbH·10886982142450·2.4MM CORTEX SCREW 3.5MM HEAD/SELF-TAPPING 7MM

    BABY DOPPLEX 4000 (BD4000)

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

    HOSPIRA INFUSION BLOOD SETS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 30, 2013

    Y-SHAPED BLOOD SET W/ PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·September 12, 2013

    MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 32 SIZE S -4

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·September 12, 2022

    Y-SHAPED BLOOD SET W/ PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code BRZ·September 13, 2013

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·August 6, 2013

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·December 17, 2013

    NDEHP Y-BLOOD SET W/FILTER PUMP 203CM

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·February 24, 2011

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·August 6, 2013

    SOLUSET 100X60W/CAI

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·December 10, 2013

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·October 27, 2014

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 11, 2011

    SOFPORT AO INTRAOCULAR LENS

    FDA Adverse Event
    Injury ·BAUSCH & LOMB·Product code HQL·June 28, 2013