BEUDAMED
    12 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    UNK SERI SURGICAL SCAFFOLD

    FDA Adverse Event
    Injury ·ALLERGAN·Product code OXF·June 25, 2014

    ARROWG+ARD CATHETER PRODUCTS

    FDA Adverse Event
    Injury ·ARROW INTL INC·Product code DQO·October 17, 2008

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP (OUS)

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·June 28, 2013

    PROMUS PREMIER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·March 11, 2026

    PENUMBRA SYSTEM 4MAX REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·May 22, 2014

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·March 3, 2016

    EDWARDS UNKNOWN SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·February 22, 2019

    EDWARDS INTRODUCER SET UNKNOWN

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·February 22, 2019

    EDWARDS UNKNOWN SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·February 22, 2019

    EDWARDS UNKNOWN SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·February 22, 2019

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 23, 2019

    SOLITAIRE FR2

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code NRY·January 30, 2015