BEUDAMED
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    Filters Status: Injury ×

    U OF I STERNUM NEEDLE 15GA

    FDA Adverse Event
    Injury ·ALLEGIANCE HEALTHCARE CORPORATION·Product code FMI·August 18, 2000

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·February 6, 2011

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON-IRVINE TECHNOLOGY CTR.·Product code HQE·November 3, 2005

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·January 6, 2011

    ENDO GIA II 60-4.8 SULU

    FDA Adverse Event
    Injury ·USSC PUERTO RICO·Product code GDW·July 13, 2011

    STYLE 410 COHESIVE SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·June 6, 2023

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON LABORATORIES INC.·Product code HQE·April 9, 1998

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQE·April 9, 1998

    MEDI-TECH

    FDA Adverse Event
    Injury ·MEDI TECH·Product code FOZ·October 23, 2002

    ASH SPLIT CATHETER

    FDA Adverse Event
    Injury ·MEDCOMP·Product code MSD·April 12, 2002

    SAF SITE

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL, INC.·Product code FPA·June 2, 1994

    COAXIAL TIP

    FDA Adverse Event
    Injury ·IOPTEX·Product code CCQ·June 26, 1995

    ALARIS PUMP PCU (BRAIN)

    FDA Adverse Event
    Injury ·BD/CAREFUSION 303, INC.·Product code FRN·July 29, 2019

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQE·December 24, 2004

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNILOGY CENTER·Product code HQE·June 6, 2002

    ST. JUDE MEDICAL

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code LWS·June 30, 2017

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON- IRVIVE TECHNOLOGY CENTER·Product code HQE·June 5, 2001

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC·Product code HQE·July 9, 1998

    FOLDALITE III 32 LAMP

    FDA Adverse Event
    Injury ·NATIONAL BIOLOGICAL CORPORATION·Product code FTC·September 2, 2021

    AMS 800 URINARY CONTROL SYSTEM WITH INHIBIZONE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EZY·July 19, 2020