BEUDAMED
    43 results · 23ms · Sources: EU EUDAMED, US FDA

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    FLAATZ 560

    FDA 510(k)
    FDA Class 2 ·Radiology

    MicroSelectron Digital

    FDA UDI
    Nucletron B.V.·08717213033542·Coupling Treatment Tube for 4F Flexibles (21)

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHE USA·Product code HWC·April 9, 2015

    SCREW, FIXATION, BONE

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

    SCREW, FIXATION, BONE

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

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·October 7, 2015

    SPIKED WASHER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SENSITITRE OPTIREAD

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·June 16, 2016

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 13, 2014

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES SELZACH·Product code HWC·June 2, 2015

    SCREW, FIXATION, BONE

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

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·July 30, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·February 15, 2017

    SCREW LOCKING

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES OBERDORF·Product code HWC·March 14, 2012

    IN TOUCH EU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 14, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 2, 2011

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·August 13, 2008