BEUDAMED
    13 results · 17ms · Sources: EU EUDAMED, US FDA

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    PVC ABDOMINAL/RECTAL PRESSURE CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517701497·BASE Trial, 14x34x24mm 15°

    JBC AND COMPANY

    FDA registration
    JBC AND COMPANY·1 product·🇺🇸 United States

    ROCKWELL MEDICAL

    FDA registration
    ROCKWELL MEDICAL·1 product·🇺🇸 United States

    RUMI II KOH-EFFICIENT

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

    HEARTECH MODEL IN TECH

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

    OPTICAL CATHETER INTRODUCER SETS, MODIFICATION

    FDA 510(k)
    FDA Class 1 ·General Hospital

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF004655295431517201·BTE-TRT

    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

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 11, 2013

    PINNACLE SECTOR II CUP 58MM

    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