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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    ULTRAFIT LINERS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    RUMI II KOH-EFFICIENT

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

    FORTEX(TM) WOUND DRESSING

    FDA 510(k)
    FDA Class 1 ·General Hospital

    FANA 60

    FDA 510(k)
    FDA Class 2 ·Immunology

    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

    MAXIMO II CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·February 11, 2013

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·January 10, 2011

    OT VERIO IQ METER

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

    TM-ECOCHGTRODE

    FDA Adverse Event
    Other ·NATUS MEDICAL INC·Product code GXY·January 9, 2009