BEUDAMED
    6,198 results · 27ms · Sources: EU EUDAMED, US FDA

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    RESTYLANE-L

    FDA Adverse Event
    Injury ·GALDERMA Q-MED AB·Product code LMH·August 26, 2021

    RESTYLANE-L

    FDA Adverse Event
    Injury ·GALDERMA Q-MED AB·Product code LMH·August 26, 2021

    JUVEDERM VOLUMA XC/LIDO (VOLUME UNKNOWN)

    FDA Adverse Event
    Injury ·PRINGY·Product code LMH·October 22, 2024

    FEMORAL HEAD IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER PRODUCT SERVICE DISTRIBUTION CENTER·Product code JDD·March 22, 1994

    HEAD

    FDA Adverse Event
    Injury ·HOWMEDICA, INC.·Product code JDD·March 31, 1994

    PRECISION FEMORAL STEM

    FDA Adverse Event
    Injury ·HOWMEDICA, INC.·Product code JDD·January 24, 1994

    44MM AUSTIN MOORE PROSTHESIS

    FDA Adverse Event
    Injury ·HOWMEDICA, INC.·Product code JDD·March 3, 1994

    BHR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW INC., ORTHOPAEDIC DIV.·Product code JDD·April 30, 2007

    BHR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC., ORTHOPAEDIC DIV.·Product code JDD·April 30, 2007

    BHR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC., ORTHOPAEDIC DIV·Product code JDD·June 13, 2007

    BHR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC., ORTHOPAEDIC DIV.·Product code JDD·April 30, 2007

    JET X

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC., ORTHOPAEDIC DIV.·Product code JDD·September 30, 2004

    PFR 12.0MM X 175MM COCR

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDD·December 20, 2005

    TITANIUM FEMORAL STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDD·November 21, 2005

    EXCEED ABT E1 FLNG CUP 28X46MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDD·April 17, 2019

    BHR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC., ORTHOPAEDIC DIV.·Product code JDD·December 7, 2007

    PCA 32MM STD FEMORAL HEAD

    FDA Adverse Event
    Injury ·HOWMEDICA, INC.·Product code JDD·October 14, 1993

    ZIMMER FEMORAL HEAD PROSTHESIS

    FDA Adverse Event
    Injury ·ZIMMER·Product code JDD·November 5, 1993

    SPECTRON EF

    FDA Adverse Event
    Injury ·SMITH & NEPHEW INC., ORTHOPAEDIC DIV.·Product code JDD·June 12, 2006

    ZIMMER

    FDA Adverse Event
    Injury ·ZIMMER·Product code JDD·July 20, 1994