BEUDAMED
    1,342 results · 175ms · Sources: EU EUDAMED, US FDA

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    FAST-FIX/IMPLANTS

    FDA Adverse Event
    Malfunction ·MANSFIELD MANUFACTURING SITE·Product code GAT·May 13, 2010

    TRUFIT BGS PLUG KITS

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW ENDOSCOPY·Product code MQV·November 1, 2010

    PRELOADED 2.8MM TI SUTURE ANCHOR W/ # 2 SUTURE

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC. ENDOSCOPY DIVIS·Product code MBI·June 20, 2001

    ACUFEX, 4.5MM CANN. ENDOSCOPIC DRILL

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC. ENDOSCOPY DIVISION·Product code HTW·July 7, 2000

    BIOSURE HA SCREW

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW MANSFIELD MANUFACTURING SITE·Product code HWC·March 22, 2012

    PRELOADED RC5 5.0MM TI SUTURE ANCHOR

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC. ENDOSCOPY DIVIS·Product code MBI·June 15, 2001

    BIORCI DRIVER

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC. ENDOSCOPY DIVISION·Product code HXX·July 3, 2001

    ULTRA FASTFIX AB CURVED NEEDLE DELIVERY SYSTEM W/SPLIT CANNULA

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW MANSFIELD MANUFACTURING SITE·Product code GAT·March 9, 2012

    DYONICS 25 CONTROL UNIT

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW OKLAHOMA CITY MANUFACTURING SITE·Product code HRX·February 21, 2012

    TABLE, OPERATING-ROOM, ELECTRICAL

    FDA Adverse Event
    Malfunction ·SMITH AND NEPHEW INC. ENDOSCOPY DIVISION·Product code GDC·October 7, 2016

    7X72MM CLEAR TRAC THREADED CANNULA

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC., ENDOSCOPY DIVISION·Product code HRX·January 30, 2009

    TWINFIX 5.0MM ANCHOR W/ULTRABRAID AND NEEDLES

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC., ENDOSCOPY DIVISION·Product code MBI·January 5, 2009

    TWINFIX TI 5.0 QUICK-T

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC., ENDOSCOPY DIVISION·Product code MBI·January 16, 2009

    TWINFIX TI 5.0 ULTRABRAID

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC. ENDOSCOPY DIVISION·Product code MBI·January 15, 2009

    ULTRA FAST-FIX AB REVERSE CURVED

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC. ENDOSCOPY DIVISION·Product code GAS·January 8, 2009

    SYNOVATOR BLADE, 4.5 DISP, EP-1

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC., ENDOSCOPY DIVISION·Product code HRX·January 21, 2009

    TWINFIX TI 5.0 PROLOADED ANCHOR W/O NEEDLES

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC. ENDOSCOPY DIVISION·Product code MBI·February 13, 2004

    ORBIT SYNOVATOR

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC., ENDOSCOPY DIVISION·Product code GEI·January 27, 2010

    DYONICS

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC., ENDOSCOPY DIVISION·Product code HRX·February 3, 2010

    DYONICS

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC., ENDOSCOPY DIVISION·Product code HRX·January 28, 2010