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

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    Filters FDA Adverse Event ×

    ACCU-CHEK FLEXLINK

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code FPA·July 20, 2007

    ACCU-CHEK FLEXLINK

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code FPA·March 29, 2007

    ACCU-CHEK FLEXLINK

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code FPA·July 20, 2007

    FOOTPRINT ULTRA PK SUTURE ANCHOR, 4.5

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·August 4, 2015

    ACCU-CHEK FLEXLINK

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code FPA·March 29, 2007

    FOOTPRINT ULTRA PK SUTURE ANCHOR, 4.5

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·July 28, 2015

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    ANI [ A&I ] GROUP TAIWAN·Product code IOR·April 3, 2013

    CROSSER RECANALIZATION CATHETER

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·March 18, 2011

    PUMP MMT-522NAS PRDGM INS V2.2 SK EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·April 24, 2008