BEUDAMED
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    Filters Status: Malfunction ×

    LID

    FDA Adverse Event
    Malfunction ·DEPUY FRANCE SAS - 3003895575·Product code FSM·September 8, 2023

    VENTRICULO-PERITONEAL SHUNT

    FDA Adverse Event
    Malfunction ·CORDIS·Product code LID·July 21, 1994

    PRIMLINE LID

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code KCT·October 2, 2018

    PRIMELINE LID

    FDA Adverse Event
    Malfunction ·AESCULAP·Product code KCT·March 19, 2014

    LID SPECULUM

    FDA Adverse Event
    Malfunction ·STORZ INSTRUMENT COMPANY·Product code HNC·September 15, 1997

    UNIVERSAL LID

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code FSM·April 17, 2026

    UNIVERSAL LID

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code FSM·April 17, 2026

    ACCULAN LID

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code HAB·March 10, 2021

    LID FOR BATTERY HANDPIECE LID FOR BATTERY HANDPIECE

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code MOQ·September 16, 2014

    STERILCONTAINER PRIMELINE LID

    FDA Adverse Event
    Malfunction ·AESCULAP, INC.·Product code KCT·May 27, 2014

    LID FOR HANDPIECE

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code MOQ·October 7, 2014

    WATER CONTAINER (LID)

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FET·June 10, 2022

    WATER CONTAINER (LID)

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code FET·April 11, 2024

    WATER CONTAINER (LID)

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FET·June 10, 2022

    WATER CONTAINER (LID)

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code FET·October 8, 2025

    SHARP CONTAINER LIDS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MMK·March 19, 2021

    ORTHOPAEDIC BIOSYSTEM LID

    FDA Adverse Event
    Malfunction ·ORTHOPAEDIC BIOSYSTEMS·Product code KGS·October 7, 2002

    LIFEPAK® CR2 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·December 16, 2021

    LIFEPAK CR2 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·August 6, 2020

    LIFEPAK(R) CR2 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·July 30, 2021