BEUDAMED
    296 results · 53ms · Sources: EU EUDAMED, US FDA

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    QUICKSEAL CONTROL

    FDA Adverse Event
    Injury ·SUB-Q, INC.·Product code MGB·January 9, 2004

    QUICKSEAL ARTERIAL CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·SUB-Q, INC.·Product code MGB·October 27, 2003

    QUICKSEAL CCS ARTERIAL CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·SUB-Q, INC.·Product code MGB·July 16, 2003

    QUICKSEAL II

    FDA Adverse Event
    Injury ·SUB-Q, INC.·Product code MGB·September 3, 2003

    QUICKSEAL CCS ARTERIAL CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·SUB-Q, INC.·Product code MGB·February 27, 2003

    QUICKSEAL SURESHOT

    FDA Adverse Event
    Injury ·SUB-Q, INC.·Product code MGB·August 11, 2004

    QUICKSEAL ARTERIAL CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·SUB-Q, INC.·Product code MGB·September 12, 2002

    QS DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·SUB-Q INC.·Product code KYZ·August 2, 2002

    QUICKSEAL CCS ARTERIAL CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·SUB-Q, INC.·Product code MGB·June 5, 2003

    QS DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·SUB-Q, INC.·Product code KYZ·June 28, 2002

    QUICKSEAL FEMORAL ARTERY CLOSURE DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·SUB-Q, INC.·Product code MGB·November 6, 2002

    QS DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·SUB-Q, INC.·Product code KYZ·November 15, 2002

    VCL+ VIO 27IN 2-0 S/A SH

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·May 21, 2020

    VCL+ UD 27IN 3-0 S/A SH

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·June 26, 2020

    BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·April 3, 2018

    Blanketrol III, Model Number 233, Cincinnati Sub-Zero Products, Inc., 12011 Mosteller Road, Cincinnati, OH 45241 Hyper-Hypothermia device used to lower or to raise a patients temperature and/or maintain a desired patient temperature through conductive heat transfer.

    FDA Recall
    Terminated ·Cincinnati Sub-Zero Products Inc·Product code DWJ·September 3, 2013

    VITROS ECI IMMUNODIAGNOSTIC SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code MMI·April 8, 2011

    NON ABSORBABLE SURGICAL SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAP·January 31, 2023

    NON ABSORBABLE SURGICAL SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAP·January 31, 2023

    MP VIAL ADAPTER 13 MM

    FDA Adverse Event
    Malfunction ·WEST PHARMA SERVICES IL, LTD·Product code LHI·September 4, 2024