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

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    SEMI-QUANTITATIVE ASSAY FOR DET. OF IGG AND IGM

    FDA 510(k)
    FDA Class 2 ·Immunology

    MODEL SF. D&SX.D PACEMAKER LEADS

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    SMITH & NEPHEW FOOTPRINT ULTRA PK SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKPALMAZCORONARY

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code MAF·April 23, 2021

    UNKNOWN PALMAZ BALLOON EXPANDABLE STENT

    FDA Adverse Event
    Injury ·CARDINAL HEALTH MEXICO·Product code FGE·April 28, 2021

    UNKPALMAZCORONARY

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code MAF·May 12, 2021

    UNKNOWN PALMAZ BALLOON EXPANDABLE STENT

    FDA Adverse Event
    Injury ·CARDINAL HEALTH MEXICO·Product code FGE·April 27, 2021

    UNKPALMAZCORONARY

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code MAF·May 12, 2021

    UNKNOWN PALMAZ BALLOON EXPANDABLE STENT

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH MEXICO·Product code FGE·April 23, 2021

    UNKPALMAZCORONARY

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code MAF·May 12, 2021

    UNKNOWN PALMAZ BALLOON EXPANDABLE STENT

    FDA Adverse Event
    Injury ·CARDINAL HEALTH MEXICO·Product code FGE·May 5, 2021

    FOOTPRINT ULTRA PK SUTURE ANCHOR, 4.5

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

    FOOTPRINT ULTRA PK SUTURE ANCHOR, 4.5

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

    PROLENE POLYPROPYLENE MESH

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·June 25, 2014

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·January 2, 2013

    PRECISE SDS SELF EXPANDING

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code FGE·November 9, 2010

    GYC-1000

    FDA Adverse Event
    Malfunction ·NIDEK CO., LTD.·Product code HQF·June 18, 2015