BEUDAMED
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    Filters FDA Adverse Event ×

    H-MAX S LATERALIZED FEMORAL STEM #14

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code MEH·December 17, 2021

    PLUM 4-PORT 15 FLTR 2CLV PE LINE 216CM

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 27, 2013

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 7, 2013

    UNKNOWN ZIMMER KNEE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·February 22, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·February 25, 2008