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

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    Filters Regulation: Us FDA ×

    CONSENSUS(TM) KNEE COBALT CHROME NONPOROUS STEMMED TIBIAL BASEPLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CENTRA HEART STATION

    FDA 510(k)

    SYRINGE FILTER DEVICES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    COULTER® LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·February 6, 2013

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 4, 2011

    SENSOR ENLITE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·July 21, 2014

    BD¿ CHOCOLATE AGAR (GC II AGAR WITH ISOVITALEX¿)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSO·July 15, 2022

    BD¿ CHOCOLATE AGAR (GC II AGAR WITH ISOVITALEX¿), PLATE, 90 MM X 120

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSO·March 29, 2022

    PLATE CHOCO GC AGAR W/ISOVITALEX 90MM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSO·June 1, 2021