BEUDAMED
    470 results · 109ms · Sources: EU EUDAMED, US FDA

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    DOBBHOFF FEEDING TUBE

    FDA Adverse Event
    THE KENDAL CO.·Product code FPD·March 21, 2002

    UNKNOWN - BLANK

    FDA Adverse Event
    THE KENDAL CO.·Product code FPD·May 21, 2002

    SCD TUBING

    FDA Adverse Event
    Malfunction ·KENDALL-SENECA·Product code JOW·August 16, 2001

    3CC-E-CMB 23G X 1

    FDA Adverse Event
    Malfunction ·TYCO HEALTHCARE/KENDALL·Product code FMF·June 15, 2004

    3CC-E-CMB 23G X 1

    FDA Adverse Event
    Malfunction ·TYCO HEALTHCARE/KENDALL·Product code FMF·June 15, 2004

    MONOJECT 450 SAL EJECTOR 3283

    FDA Adverse Event
    Malfunction ·TYCO HEALTHCARE/KENDALL·Product code DZM·June 6, 2005

    MONOJECT 418 DENTAL INJECTOR 27SH

    FDA Adverse Event
    Malfunction ·TYCO HEALTHCARE/KENDALL·Product code DZM·June 7, 2005

    VISTEC XRAY DETECTABLE SPONGES

    FDA Adverse Event
    Malfunction ·KENDALL/TYCO·Product code GDY·April 26, 2006

    COVIDIEN/KENDALL

    FDA Adverse Event
    Injury ·15 HAMPSHIRE STREET·Product code MPB·May 5, 2009

    KENDALL

    FDA Adverse Event
    Malfunction ·THE KENDALL CO·Product code GAA·March 31, 2004

    250E NDL 25 X 5/8 A

    FDA Adverse Event
    Other ·THE KENDALL CO·Product code FMF·August 22, 2003

    FOLY CATH 100% SLCON 30CC 20FR

    FDA Adverse Event
    THE KENDALL CO.·Product code EZL·September 15, 2003

    MONOJECT MONOLETTER

    FDA Adverse Event
    Other ·THE KENDALL CO.·Product code FMK·September 16, 2003

    KENDALL

    FDA Adverse Event
    Malfunction ·THE KENDALL CO.·Product code FCE·August 2, 2000

    KENDALL

    FDA Adverse Event
    Death ·THE KENDALL CO.·Product code LFJ·August 9, 2000

    KENDALL WEBCOL ALCOHOL PREP

    FDA Adverse Event
    Malfunction ·THE KENDALL CO.·Product code LKB·April 11, 2000

    MONOJECT SYRINGE

    FDA Adverse Event
    Malfunction ·THE KENDALL CO.·Product code FMF·June 9, 2000

    HYPODERMIC NEEDLES (MONOJECT)

    FDA Adverse Event
    Malfunction ·THE KENDALL CO.·Product code GAA·April 7, 2000

    CURITY ULTRAMER CATHETER

    FDA Adverse Event
    Other ·THE KENDALL CO·Product code KOD·May 11, 2000

    ARYGLE TURKEL SAFETY THORACENTESIS PROCEDURE TRAY

    FDA Adverse Event
    Malfunction ·THE KENDALL CO.·Product code KDQ·May 24, 2000