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

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    NEEDLE INFOR NOT AVAILABLE

    FDA Adverse Event
    Other ·Product code GAB·March 19, 2009

    ETHICON CHROMIC GUT 1 CT NEEDLE

    FDA Adverse Event
    Other ·ETHICON INC·Product code GAB·February 13, 2004

    TORRINGTON DISPOSABLE STERILE STAINLESS STEEL SURGEONS' NEEDLES

    FDA Adverse Event
    Other ·HOSPITAL MARKETING SERVICES, CO, INC.·Product code GAB·May 22, 2012

    ASPEN SURGICAL PRODUCTS

    FDA Adverse Event
    Other ·ASPEN SURGICAL PRODUCTS·Product code GAB·August 22, 2003

    ETHICON SYNTHETIC SUTURE NEEDLE

    FDA Adverse Event
    Other ·ETHICON, INC.·Product code GAB·March 9, 1994

    CONTOUR

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP.·Product code GAB·May 25, 2007

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAB·November 26, 2008

    RICHARD ALLEN SURGICAL NEEDLE

    FDA Adverse Event
    Other ·ASPEN SURGICAL PRODUCTS, INC.·Product code GAB·February 21, 2013

    RICHARD ALLEN SURGICAL NEEDLE

    FDA Adverse Event
    Other ·ASPEN SURGICAL PRODUCTS, INC.·Product code GAB·February 22, 2013

    ELITE PASS SUTURE SHUTTLE NEEDLE

    FDA Adverse Event
    Other ·SMITH AND NEPHEW, INC., ENDOSCOPY·Product code GAB·October 14, 2009

    ETHICON

    FDA Adverse Event
    Other ·ETHICON·Product code GAB·May 26, 2005

    ETHICON

    FDA Adverse Event
    Other ·ETHICON - J & J·Product code GAB·January 3, 2003

    UNK

    FDA Adverse Event
    Other ·ETHICON, INC.·Product code GAB·July 29, 1998

    ETHICON

    FDA Adverse Event
    Other ·ETHICON, INC·Product code GAB·August 22, 2002

    SUTURE NEEDLE

    FDA Adverse Event
    Other ·ETHICON, INC.·Product code GAB·October 11, 1995

    SUTURE NEEDLE

    FDA Adverse Event
    Other ·ETHICON, INC.·Product code GAB·November 2, 1995

    ETHICON

    FDA Adverse Event
    Other ·ETHICON·Product code GAB·June 18, 2003

    SUTURE NEEDLE

    FDA Adverse Event
    Other ·ETHICON, INC.·Product code GAB·February 4, 1997

    1824347-1997-00001

    FDA Adverse Event
    Other ·Product code GAB·March 12, 1997

    SUREFIRE SCORPION NEEDLE

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code GAB·May 14, 2008