BEUDAMED
    26 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    VASCO TIP BI 9/58

    FDA Adverse Event
    Malfunction ·VASCO MED·Product code DTB·June 16, 1999

    GROSHONG 4 FR MIDLINE

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code DQO·March 1, 1999

    B-D 10 ML SYRINGE LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO.·Product code FMI·March 1, 1999

    AUTO SUTURE MULTIFIRE GIA 80-4.8

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP·Product code GAG·May 20, 1998

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·July 23, 1999

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·February 17, 1999

    AUTO SUTURE PREMIUM SURGICLIP M-9.75

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAG·June 19, 1998

    AUTO SUTURE ILA 100 DISPOSABLE LOADING UNIT

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAG·May 26, 1998

    AUTO SUTURE ROTICULATOR 30-V3

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP·Product code GAG·June 25, 1998

    LP10 VOLUME VENTILLATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·November 24, 1999

    AUTO SUTURE ENDO UNIVERSAL 65-4.0

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORPORATION·Product code GCJ·February 3, 1998

    AUTO SUTURE ENDO CLIP 5MM

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GCJ·March 25, 1998

    AUTO SUTURE ENDO CATCH 10MM

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GCJ·June 11, 1998

    ABBOTT AXSYM SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·August 19, 1999

    CAPNO-FLO

    FDA Adverse Event
    Malfunction ·KIRK SPECIALTY SYSTEMS·Product code BTM·June 7, 1999

    B-D 3ML 23G NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO.·Product code FMF·July 15, 1999

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LKK·December 13, 1999

    S.SCORT DUET

    FDA Adverse Event
    Malfunction ·SSCOR, INC.·Product code BTA·February 12, 1999

    HEMASHIELD KNITTED DOUBLE VELOUR FABRIC

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC/VASCULAR·Product code DXZ·December 16, 1999

    SHILEY FENESTRATED LOW PRESSURE CUFFED TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·MALLINCKRODT MEDICAL, INC.·Product code BTO·September 2, 1999