BEUDAMED
    20 results · 40ms · Sources: EU EUDAMED, US FDA

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    HYALGAN

    FDA Adverse Event
    Injury ·FIDIA SPA·Product code MOZ·March 17, 2000

    HEP-LOCK

    FDA Adverse Event
    WYETH-AYERST LABORATORIES·Product code FMF·February 28, 2002

    NORPLANT SYSTEM

    FDA Adverse Event
    WYETH - AYERST LABORATORIES·Product code MFH·January 22, 1993

    SYNVISC HYLAN G-F-20

    FDA Adverse Event
    Injury ·BIOMATRIX, INC. WYETH AYERST LABORATORIES·Product code MOZ·July 23, 2001

    SYNVISC 8 MG/CC

    FDA Adverse Event
    Injury ·WYETH-LABORATORIES DIV. WYETH-AYERST PHARMACEUTICALS·Product code MOZ·May 3, 2000

    SYNVISC 8 MG/CC

    FDA Adverse Event
    Other ·WYETH-LABORATORIES DIV. WYETH-AYERST PHARMACEUTICALS·Product code MOZ·May 3, 2000

    SYNVISC 8 MG/ML

    FDA Adverse Event
    Injury ·WYETH-LABORATORIES DIV. WYETH - AYERST PHARMACEUTICALS·Product code MOZ·May 1, 2000

    SYNVISC 8MG/CC

    FDA Adverse Event
    Other ·WYETH-LABORATORIES DIV. WYETH AYERST PHARMACEUTICALS·Product code MOZ·May 4, 2000

    SYNVISC 8 MG/CC

    FDA Adverse Event
    Other ·WYETH-LABORATORIES DIV. WYETH-AYERST PHARMACEUTICALS·Product code MOZ·May 3, 2000

    THIN VISC

    FDA Adverse Event
    Injury ·WYETH LABORATORIES, INC. DIV. OF WYETH-AYERST PHARMACEUTICALS·Product code MOZ·October 7, 1999

    VITEK MS INSTRUMENT

    FDA Adverse Event
    Malfunction ·BIOMÉRIEUX, SA·Product code QBN·October 14, 2021

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·December 28, 2018

    BACT/ALERT® FA PLUS CULTURE BOTTLE

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·October 10, 2018

    OT ULTRASMART METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·September 14, 2007

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 10, 2013

    COMPLETE MOISTUREPLUS

    FDA Adverse Event
    Injury ·ADVANCED MEDICAL OPTICS, INC.·Product code LPN·July 28, 2006

    EVIS LUCERA ELITE COLONOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·April 19, 2024

    PLATE COLUMBIA AG 5PRCT SB 90MM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code KZI·November 2, 2021

    ADVANTAGE FIT? BLUE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code OTN·May 14, 2025

    BACT/ALERT FA PLUS (PLASTIC)

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code MDB·October 8, 2021