BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    AIA-PACK IGE II ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    NORMAL GLOBULIN REAGENT

    FDA 510(k)
    FDA Class 2 ·Immunology

    3T BLOOD COLLECTION CARDIOTOMY RESERVOIRS AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IBP ELBOW INTERLOK FINISH ULNAR COMPONENT STANDARD LEFT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·June 14, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·February 9, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·March 2, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·February 9, 2017

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·February 21, 2013

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FPA·January 20, 2011

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·August 1, 2014

    LIGACLIP ENDOSCOPIC MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDO·May 29, 1997