BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    MULTI-PURPOSE CONTROL SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ANGIOMED RENAL DILATION SET

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BCYE AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    M2A 38MMX50MM CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018

    M2A 38MM MOD HD+9MM NK NO SKRT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018

    UNICEL DXC 600 PRO SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·June 19, 2014

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code JDI·October 22, 2010

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·December 26, 2012

    XP-XP Tibial Tray - Interlok 83 mm Item # 195759

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·September 18, 2019