BEUDAMED
    13 results · 21ms · Sources: EU EUDAMED, US FDA

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    SUCTION INSTRUMENTATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    artegral

    FDA UDI
    Merz Dental GmbH·D7091972074·posteriors; shade B3; size M; upper jaw

    MODEL 674 PACER ANALYZER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RADIAL IMMUNODIFFUSION KIT-TRANSFERRIN

    FDA 510(k)
    FDA Class 2 ·Immunology

    BD VACUTAINER PPT PLASMA PREPARATION TUBE K2E 9.0 MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·May 7, 2018

    BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·April 26, 2018

    SEE H10

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 17, 2020

    BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·April 26, 2018

    BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·April 26, 2018

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·February 21, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·January 27, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·July 31, 2014

    BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·July 17, 2018