BEUDAMED
    10 results · 25ms · Sources: EU EUDAMED, US FDA

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    PRESSURE SORE MANAGEMENT KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123137·K-WIRE - DOUBLE TROCAR 1.1mm DIA x 150mm

    ACRYDERM SILVER ANTIMICROBIAL PERFORATED WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    DIGITAL CLINICAL THERMOMETER MODEL V901US

    FDA 510(k)
    FDA Class 2 ·General Hospital

    8015 ALARIS SYSTEM PC UNIT

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·January 7, 2021

    BD DISCARDIT II SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 2, 2020

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·July 10, 2015

    70 DEGREE CURVED SUCTION, EM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·January 11, 2013

    PFNA-II Ø10 SM 130° L200 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES BETTLACH·Product code HSB·July 3, 2014

    PROTECTOR SOLUS P120J

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·March 10, 2020