BEUDAMED
    18 results · 25ms · Sources: EU EUDAMED, US FDA

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    SYNTHETIC VINYL PATIENT EXAMINATION GLOVES-POWDER FREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496040682·CORSARO, SIZE S, MOKA, MICRO-MASSAGING CAPRI PA...

    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

    HELAX-TMS V 5.1 RADIATION THERAPY TREATMENT PLANNING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    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

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·April 8, 2013

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·March 22, 2011

    ASCENSIA BREEZE2 TEST STRIPS (30)

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·May 8, 2008

    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

    The Spirit Select Bed, Model 5700 Spirit Plus /with high rail siderail option

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·November 21, 2018