BEUDAMED
    9 results · 40ms · Sources: EU EUDAMED, US FDA

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    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·July 20, 2021

    CUP: MPACT ACETABULAR SHELL Ø52 TWO-HOLES

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·April 10, 2024

    LINER: MPACT FLAT PE HC LINER 36/G

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·September 7, 2021

    KAPPA DDDR 900

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code DXY·October 9, 2020

    STERRAD NX STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·October 4, 2016

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·March 2, 2011

    SLIDING CORE UHMPWE, 7MM

    FDA Adverse Event
    Injury ·STRYKER GMBH·Product code NTG·October 21, 2021