BEUDAMED
    8 results · 34ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    PICCOLO BASIC METABOLIC PANEL

    FDA Adverse Event
    Malfunction ·ABAXIS, INC.·Product code CGX·October 22, 2020

    PICCOLO COMPREHENSIVE METABOLIC PANEL

    FDA Adverse Event
    Malfunction ·ABAXIS, INC.·Product code CGX·November 3, 2020

    GII QA+ O/C CP-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·January 29, 2019

    GII QA+ O/C CP-2 *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code JDR·January 29, 2019

    HS III PROXIMAL SEAL SYTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·May 13, 2014

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·January 11, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·December 2, 2010

    ORTHOPEDIC SALVAGE SYSTEM ARCOM LS TIBIAL BEARING 12MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·July 20, 2022