BEUDAMED
    37 results · 24ms · Sources: EU EUDAMED, US FDA

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    APPLIANCE, FIXATION, NAIL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KTT·August 18, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·January 5, 2016

    SYNTHES LARGE FRAGMENT DYNAMIC COMPRESSION LOCKING (DCL) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES BETTLACH·Product code HWC·September 23, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES MEZZOVICO·Product code HWC·September 1, 2015

    LCP 4.5/5 BROAD 18HO L332 TI

    FDA Adverse Event
    Injury ·SYNTHES·Product code KTT·December 12, 2012

    LOCKSCR Ø5 SELF-TAP L55 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code KTT·April 11, 2013

    LOCKSCR Ø5 SELF-TAP L40 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code KTT·June 27, 2013

    LOCKSCR Ø5 SELF-TAP L44 TAN

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code KTT·October 18, 2013

    APPLIANCE,FIXATION,NAIL

    FDA Adverse Event
    Injury ·SYNTHES BETTLACH·Product code KTT·October 10, 2016

    2.5MM DRILL BIT/QC/GOLD/110MM

    FDA Adverse Event
    Malfunction ·SYNTHES GRENCHEN·Product code KTT·September 5, 2017

    CUSTOM PROCEDURE KIT

    FDA UDI
    MEDIVATORS INC.·40677964006126·The ENDO CARRY-ON Procedure Kit contains all of...

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65810006821·ENGINE FILES 21MM

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·10304040134532·Engine Files 21mm

    PenEvac1

    FDA UDI
    I.C. MEDICAL, INC.·00817688023920·PenEvac1, Non-Stick Blade, 14-Foot Tube, 15-Foo...

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·February 18, 2025

    HARDYDISK TOBRAMYCIN, 10MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    MODIFICATION TO AUTOJECT MINI

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AUTOSOFT XC

    FDA Adverse Event
    Injury ·UNOMEDICAL A/S·Product code FPA·July 17, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL UM-D·Product code FPA·January 28, 2025