BEUDAMED
    2,651 results · 39ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    BAXTER HEYER-SCHULTZE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code LID·August 28, 1994

    UNKNOWN

    FDA Adverse Event
    Injury ·UNKNOWN·Product code LID·July 18, 1994

    TUFFLITE LIDS

    FDA Adverse Event
    Injury ·AESCULAP·Product code FLE·December 9, 1996

    ATTUNE TRAY LID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.-1818910·Product code LXH·June 26, 2014

    OCUSOFT LID SCRUB

    FDA Adverse Event
    Injury ·OCUSOFT INC.·Product code HOZ·December 15, 2020

    OCUSOFT LID SCRUB

    FDA Adverse Event
    Injury ·OCUSOFT INC.·Product code HOZ·August 4, 2010

    BD¿ SHARPS COLLECTOR 3.1 FUNNEL CAP

    FDA Adverse Event
    Injury ·BECTON DICKINSON·Product code MMK·August 21, 2017

    SYSMEX CA-1500 CP

    FDA Adverse Event
    Injury ·SYSMEX CORPORATION·Product code GKP·March 21, 2016

    SIGNA EXPLORER

    FDA Adverse Event
    Injury ·GE HEALTHCARE (TIANJIN) COMPANY LIMITED·Product code LNH·May 11, 2021

    LID FOR OUTER CASES

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code FSM·April 11, 2021

    OCUSOFT LID SCRUB PLUS

    FDA Adverse Event
    Injury ·UNKNOWN·Product code HOZ·August 11, 2023

    OCUSOFT LID SCRUB PLUS

    FDA Adverse Event
    Injury ·OCUSOFT, INC·Product code HOZ·July 31, 2020

    OCUSOFT LID SCRUB PLUS

    FDA Adverse Event
    Injury ·UNKNOWN·Product code HOZ·August 11, 2023

    OTC OCUFOFT LID SCRUB

    FDA Adverse Event
    Injury ·OCUSOFT INC.·Product code HOZ·May 7, 2019

    UNKNOWN PUREWICK URINE COLLECTION SYSTEM

    FDA Adverse Event
    Injury ·C.R. BARD INC. (COVINGTON) -1018233·Product code NZU·August 21, 2025

    LOW TEMPERATURE STERILIZERS

    FDA Adverse Event
    Injury ·STERIS CORPORATION·Product code FLE·August 25, 2006

    PRO-TEC

    FDA Adverse Event
    Injury ·STC PLASTICS, INC.·Product code MMK·March 26, 2004

    TISSUE-TEK AUTOTEC® A120 AUTOMATED EMBEDDING SYSTEM

    FDA Adverse Event
    Injury ·SAKURA SEIKI CO., LTD.·Product code IEO·October 20, 2023

    RIATA ST ACTIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·August 21, 2006

    STERIS SYSTEM 1

    FDA Adverse Event
    Injury ·STERIS CORPORATION - HOPKINS·Product code MED·April 6, 2010