BEUDAMED
    11 results · 30ms · Sources: EU EUDAMED, US FDA

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    CONVEEN EASICATH SET

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

    PRESTIGE® LP Cervical Disc System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994714855·INNER SHAFT 6973070 7MM INSERTER US

    artegral HD

    FDA UDI
    Merz Dental GmbH·D7091973070·posteriors; shade B3; size XL; upper jaw

    HSW Resection Instruments

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

    DIO BIOTITE-H IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    ARCHITECT CREATINE KINASE

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code CGS·July 21, 2018

    ARCHITECT CREATINE KINASE

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code CGS·July 21, 2018

    ARCHITECT CREATINE KINASE

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code CGS·July 21, 2018

    UNIVERSAL MODULAR ELECTRIC/BATTERY DOUBLE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL S.A.·Product code GEY·April 29, 2014

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 21, 2013

    COULTER ® LH750

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code GKZ·January 28, 2011