BEUDAMED
    10,000 results · 257ms · Sources: EU EUDAMED, US FDA

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    GLUMA COMFORT OND + DESENSITIZER

    FDA Adverse Event
    Injury ·HERAEUS KULZER GMBH & CO. KG, MEDICAL DIVISION·Product code KLE·May 6, 2013

    PORT ACCESS NEEDLE

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS, INC.·Product code FPA·April 4, 2017

    GROSHONG

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS·Product code DQO·October 30, 2001

    PORT ACCESS NEEDLE

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS, INC.·Product code FPA·February 28, 2017

    D-H.E.L.P.

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code GCJ·August 12, 2014

    IKARIA

    FDA Adverse Event
    Injury ·IKARIA·Product code MRN·October 12, 2010

    ADVIA 1800

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·March 4, 2013

    KCI ATMOS AIR

    FDA Adverse Event
    Malfunction ·KCI·Product code INX·December 22, 2014

    INSIGNIA ULTRA

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS·Product code DXY·November 14, 2005

    D-DIMER 25 TEST KIT

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO INC.·Product code GHH·September 1, 2011

    PERITONEAL DIALYSIS CATHETER

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code FJS·August 12, 2023

    SYSTEM 95

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 9, 1999

    NA

    FDA Adverse Event
    Injury ·Product code KNT·December 27, 2007

    AUTOCAT2 WAVE

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DSP·February 27, 2009

    AUTO SUTURE VERSAPORT RPF 5-12MM

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP·Product code GCJ·November 20, 1997

    INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·December 16, 2025

    BD PYXIS¿ MEDSTATION¿ ES AUXILIARY

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·May 2, 2025

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC(PR)·Product code NIQ·May 8, 2006

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·May 8, 2006

    PROMUS PREMIER SELECT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·February 11, 2020