BEUDAMED
    47 results · 29ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    BVI BEAVER XSTAR SAFETY SLIT KNIFE

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL, INC.·Product code HNN·October 9, 2025

    ARCH KOH-EFFICIENT 4.0 CM ASSOCIATED HANDLE: ADVINCULA ARCH HANDLE

    FDA Adverse Event
    Malfunction ·COOPER SURGICAL INC.·Product code HEW·December 8, 2025

    ATLAS GOLD

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·June 18, 2024

    PTFE FELT PLEDGETS

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DXZ·March 15, 2023

    PTFE FELT PLEDGETS

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DXZ·April 4, 2023

    MAGNUM INSTRUMENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·November 18, 2022

    ROTAREX

    FDA Adverse Event
    Malfunction ·STRAUB MEDICAL AG·Product code MCW·August 22, 2024

    SOFTCLIX PLUS LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·April 21, 2008

    BD SYRINGE WITH NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code FMF·August 7, 2023

    POWERLINE CV CATHETER, POLYURETHANE SINGLE-LUMEN, 5F

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·May 23, 2024

    ULTRAVERSE RX

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code LIT·October 7, 2024

    CLEARLINK CONTINU-FLO SOLUTION SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·September 12, 2022

    POWERLINE CV CATHETER, POLYURETHANE SINGLE-LUMEN, 6F

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·January 31, 2024

    PEN NEEDLE AUTOSHIELD DUO 30GX5MM EU

    FDA Adverse Event
    Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·January 15, 2025

    ROTAREX

    FDA Adverse Event
    Malfunction ·STRAUB MEDICAL AG·Product code MCW·September 5, 2024

    ATLAS

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·September 1, 2024

    POWERLINE CV CATHETER, POLYURETHANE SINGLE-LUMEN, 6F

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·December 20, 2023

    ROTAREX

    FDA Adverse Event
    Malfunction ·STRAUB MEDICAL AG·Product code MCW·September 18, 2024

    ATLAS GOLD

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·July 10, 2024

    VACCESS

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code LIT·July 15, 2024