BEUDAMED
    7,387 results · 59ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    CITATION TMZF HA STEM #7 LEFT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·June 5, 2014

    WRIGHT MEDICAL PROFEMUR Z, MODULAR NECK

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL·Product code KWA·September 19, 2011

    REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 11

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 5, 2022

    25MM MOD REV HIP BODY/BOLT STDCOMPONENT LEVEL 9006-1-025

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·August 18, 2025

    WRIGHT MEDICAL MICROPORT RENAISSANCE MODULAR COCR NECK

    FDA Adverse Event
    Injury ·MICROPORT / WRIGHT MEDICAL·Product code LZO·February 26, 2020

    LRG TAP PRI MOD NCK 8DEG 34MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 5, 2022

    CONSERVE® A-CLASS® BFH® HEAD MEDIUM NECK 44MM

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code KWA·January 26, 2022

    DYNASTY® COCR LINER

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·January 26, 2022

    HEARTMATE 3

    FDA Adverse Event
    Injury ·ABBOTT·Product code DSQ·December 9, 2025

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWY·January 22, 2013

    PROFEMUR® NECK VAR/VAL 8DG LONG COBALT CHROME

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDI·December 31, 2021

    PROFEMUR® TL STEM SZ 6

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDI·December 31, 2021

    PROFEMUR® MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LWJ·January 26, 2022

    UNKNOWN TIBIAL BASEPLATE - MRH KNEE

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KRO·October 23, 2025

    M2A 38MM MOD HEAD STD NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 2, 2015

    REACH 13X200 RT 100% POR FEMORAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·March 2, 2015

    UNKNOWN REJUVENATE STEM SIZE 8

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·May 6, 2021

    UNKNOWN REJUVENATE NECK 8 ANTEVERTED

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·May 6, 2021

    M2A-MAGNUM MODULAR HEAD SZ 50MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·September 26, 2012

    SELEX/MAGNUM MODULAR HEAD 40MM +6

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·September 26, 2012