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

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    RUMI II KOH-EFFICIENT

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code HEW·October 20, 2022

    KOH COLPOTOMIZER SYSTEM

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

    KOH-EFFICIENT,RUMI

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code HEW·November 4, 2022

    KOH-EFFICIENT,RUMI

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code HEW·November 3, 2022

    EARLENS

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    RHEUMAGEN ASO T-CONTROL

    FDA 510(k)
    FDA Class 1 ·Microbiology

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF004655295431117201·BTE-TRT

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code DXY·February 11, 2013

    S- ROM SLEEVE PRX ZTT, 18B-SML

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·January 5, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2014