BEUDAMED
    50 results · 61ms · Sources: EU EUDAMED, US FDA

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    VIOS LC PLUS AEROSOL DELI

    FDA Adverse Event
    Malfunction ·PARI RESPIRATORY EQUIPMENT, INC./PRE HOLDING, INC.·Product code CAF·February 10, 2025

    FS DISPOSABLE INTERFACE

    FDA Adverse Event
    Malfunction ·AMO MANUFACTURING USA, LLC·Product code GEX·March 24, 2022

    ORTHO SUMMIT PLUS

    FDA Adverse Event
    Malfunction ·HAMILTON BONADUZ AG·Product code JTC·September 1, 2009

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·March 29, 2018

    PROKERA

    FDA Adverse Event
    Injury ·BIOTISSUE HOLDINGS INC.·Product code NQB·March 18, 2026

    *

    FDA Adverse Event
    Other ·MAQUET S.A.·Product code FSY·October 3, 2008

    *

    FDA Adverse Event
    Other ·MAQUET S.A.·Product code FSY·October 3, 2008

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·May 21, 2023

    INTRALASE FS2

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HNO·February 14, 2019

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·November 12, 2025

    BARD® TOUCHLESS® PLUS UNISEX PRE-LUBRICATED VINYL URETHRAL CATHETER KIT

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FCM·October 1, 2018

    BARD® TOUCHLESS® PLUS UNISEX PRE-LUBRICATED VINYL URETHRAL CATHETER KIT

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FCM·August 8, 2018

    INTRALASE FS2

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HNO·December 17, 2019

    SHOCKWAVE C2 CORONARY INTRAVASCULAR LITHOTRIPSY (IV) CATHETER

    FDA Adverse Event
    Injury ·SHOCKWAVE MEDICAL, INC.·Product code QMG·February 14, 2023

    BARD® TOUCHLESS® PLUS UNISEX PRE-LUBRICATED VINYL URETHRAL CATHETER KIT

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FCM·August 8, 2018

    BARD® TOUCHLESS® PLUS UNISEX PRE-LUBRICATED VINYL URETHRAL CATHETER KIT

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FCM·August 27, 2018

    DECANAV ELECTROPHYSIOLOGY CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DRF·May 23, 2024

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 10, 2026

    TECNIS IOL

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code MJP·June 27, 2025

    FS DISPOSABLE INTERFACE

    FDA Adverse Event
    Injury ·AMO MANUFACTURING USA, LLC·Product code GEX·September 3, 2021