BEUDAMED
    41 results · 38ms · Sources: EU EUDAMED, US FDA

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    BEAVER-VISITEC INTERNATIONAL INC

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL INC·Product code HMX·April 29, 2024

    LIFELINE

    FDA Adverse Event
    Malfunction ·DEFIBTECH, L.L.C.·Product code MKJ·July 26, 2024

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·November 30, 2009

    GMK SPHERE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·June 6, 2025

    TAC-S MICRO VULCAN ANGLED INTEGRATED

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code GEI·October 16, 2023

    EASYTOUCH

    FDA Adverse Event
    Malfunction ·BERPU MEDICAL TECHNOLOGY CO., LTD·Product code FMF·August 22, 2023

    QUILL SRS

    FDA Adverse Event
    Malfunction ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·September 3, 2008

    SYRINGE 0.3ML 31GA 6MM HALFUNIT 10BAGSLA

    FDA Adverse Event
    Malfunction ·EMBECTA MEDICAL I LLC - HOLDREGE, NE·Product code FMF·April 7, 2025

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·March 26, 2013

    GOBED II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·March 10, 2011

    DTC MARGRON HIP REPLACEMENT SYSTEM

    FDA Adverse Event
    Injury ·PORTLAND ORTHOPAEDICS LTD.·Product code LPH·April 1, 2008

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·May 12, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·February 13, 2009

    ANGLED REAMER, DRIVE SHAFT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·November 17, 2023

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP (DBA ANGIOTECH)·Product code NEW·March 15, 2010

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009

    QUILL KNOTLESS TISSUE-CLOSURE DEVICE

    FDA Adverse Event
    Injury ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·May 11, 2011

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·July 26, 2012

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 19, 2010

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·May 12, 2009