BEUDAMED
    12 results · 28ms · Sources: EU EUDAMED, US FDA

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    PATIENT RESTRAINTS

    FDA 510(k)
    FDA Class 1 ·General Hospital

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970275·anteriors; shade C1; mould IM

    FLEXIBLE LOOP ELECTROSURGICAL ELECTRODE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Tri Auto ZX2

    FDA 510(k)
    FDA Class 1 ·Dental

    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

    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

    X SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 29, 2014

    LCS 3 PEG ROT PATELLA CEM STD

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code HTG·February 20, 2013

    HER OPTION PROBE

    FDA Adverse Event
    Injury ·COOPERSURGICAL·Product code GEH·January 14, 2011

    BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG

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