BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNKNOWN FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code MEH·August 31, 2017

    MULTILOCK FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDI·June 30, 2016

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 27, 2013

    SECURE 2 MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·March 10, 2011

    PRECISION XTRA /OPTIUM

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·March 27, 2008

    ASAHI PROWATER

    FDA Adverse Event
    Injury ·ASAHI INTECC CO., LTD.·Product code DQX·June 9, 2019

    ASAHI PROWATER

    FDA Adverse Event
    Injury ·ASAHI INTECC CO., LTD.·Product code DQX·June 9, 2019

    SURSHIELD PUR SAFETY I.V. CATHETER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION - KOFU·Product code FOZ·December 22, 2017