BEUDAMED
    42 results · 54ms · Sources: EU EUDAMED, US FDA

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    BIOLOX D MOD CER HD 32MM STD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·December 7, 2020

    OXF UNI TIB TRAY SZA LM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·December 7, 2020

    RHK BEARING 12 FOR 63-67 TRAY

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HRY·October 16, 2020

    OXF ANAT BRG LT SM SIZE 3 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·December 7, 2020

    OXFORD UNI TWIN-PEG FEMORAL SM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·December 7, 2020

    DELTA CER FEM HD 28/-3MM T1

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code OQG·December 15, 2020

    RHK RIGHT SML RESURF FEMUR R

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·October 16, 2020

    RHK SHORT HINGE ASSEMBLY

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HRY·October 16, 2020

    EXCEED ABT E1 MULLER CUP 28X48

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·May 18, 2020

    TI-SCREW, STANDARD, SYS4.0, TX10, 32MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HRS·April 16, 2018

    BIOMET BONE CEMENT R 1X40 US

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·January 28, 2022

    BIOMET BONE CEMENT R 1X40 US

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LOD·January 28, 2022

    ACUSON ACUNAV 8F-90 ULTRASOUND CATHETER

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code OBJ·December 1, 2017

    ACUSON ACUNAV 8F-90 ULTRASOUND CATHETER

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code OBJ·December 1, 2017

    IMPELLA

    FDA Adverse Event
    Malfunction ·ABIOMED, INC. - 1220648·Product code OZD·April 10, 2026

    UNKNOWN LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 24, 2017

    KIMGUARD ONESTEP* QUICK CHECK* STERILIZATION WRAP, KC 600, 45IN X 45IN

    FDA Adverse Event
    Malfunction ·O&M HALYARD, INC.·Product code FRG·May 23, 2023

    UNKNOWN HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·March 24, 2017

    UNKNOWN LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·March 24, 2017

    UNKNOWN HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·March 24, 2017