BEUDAMED
    25 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 12, 2008

    ARVATI

    FDA Adverse Event
    Injury ·SPINESMITH HOLDINGS,LLC·Product code DWG·November 19, 2023

    T2 A/R FE NAIL

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL/STRYKER TRAUMA GMBH KIEL OPERATIONS·Product code JDS·July 15, 2004

    DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 12, 2008

    STAINLESS STEEL ELECTRODE, REUSABLE, 10CM

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·November 25, 2015

    DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 12, 2008

    GORE VIATORR® TIPS ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIR·October 2, 2018

    SINGLE-SITE

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·June 24, 2022

    SINGLE-SITE

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·September 1, 2022

    SINGLE-SITE

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·August 20, 2022

    SUREFORM

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code GDW·August 19, 2022

    NONE

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·September 2, 2022

    ZIMMER BIOMET CRUCIATE STEM PUNCH

    FDA Adverse Event
    Injury ·ZIMMERBIOMET CHILE DFE·Product code HWP·June 2, 2022

    TIMESH

    FDA Adverse Event
    Injury ·GFE MEDIZINTECHNIK GMBH·Product code FTL·July 27, 2009

    TIMESH

    FDA Adverse Event
    Injury ·GFE MEDIZINTECHNIK GMBH·Product code FTL·July 27, 2009

    TIMESH

    FDA Adverse Event
    Injury ·GFE MEDIZINTECHNIK GMBH·Product code FTL·July 27, 2009

    TIMESH

    FDA Adverse Event
    Injury ·GFE MEDIZINTECHNIK GMBH·Product code FTL·July 27, 2009

    PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/

    FDA Adverse Event
    Injury ·ZIMMER BIOMET CANADA DFE·Product code JWH·November 21, 2025

    TOTAL KNEE REPLACEMENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET AMERICAS DFE·Product code JWH·June 5, 2019

    OXFORD UNI KNEE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET CANADA DFE·Product code JWH·December 17, 2019