BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SMR GLENOSPHERE Ø 36MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·September 20, 2022

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·May 31, 2007

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 26, 2013

    EON RECHARGEABLE IPG

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·February 8, 2011

    CONTINUUM ACETABULAR SHELL WITH CLUSTER HOLES

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 7, 2018

    KINECTIVE TECHNOLOGY MODULAR NECK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 7, 2018

    NEUTRAL LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·June 7, 2018

    SELF TAPPING BONE SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 7, 2018

    EB EXC GRN 8X18IN 0 S/A CT-1 CR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAT·March 13, 2020

    EB EXC GRN 8X18IN 0 S/A CT-1 CR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAT·March 13, 2020