BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    BORRELIA BURGDORFERI IGG WESTERN BLOT TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    11G BLADED MAMMOTOME ST PROBE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.·Product code KNW·February 27, 2006

    MINITAPE URETHRAL SLING

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

    Electronic Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD VACUTAINER® CTAD BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 4, 2018

    BD VACUTAINER® CTAD BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 31, 2018

    BD VACUTAINER® CTAD BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 3, 2018

    MINICAP TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·March 6, 2013

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014

    KINAIR

    FDA Adverse Event
    Death ·KCI USA, INC.·Product code IOQ·February 11, 2011