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

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    Filters Regulation: Us FDA ×

    ULTROID HEMORRHOID MANAGEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·34546540602641·Bone Screws, emergency, MP, Cross-Pin

    HORIZONS HOT BIOPSY FORCEPS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    EBV-VCA IGG ELISA TEST, MODEL EBG-100

    FDA 510(k)
    FDA Class 1 ·Microbiology

    NONE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·September 3, 2008

    SYNCHRO 14 NEURO GUIDEWIRE

    FDA Adverse Event
    Injury ·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORPORATION·Product code DQX·July 24, 2007

    ARTICULEZE M HEAD 36MM +12

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·August 15, 2013

    PINNACLE MTL INS NEUT36IDX60OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·August 15, 2013

    SYNCHRO -10 NEURO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIV·Product code DQX·December 15, 2006

    SYNCHRO-14 NEURO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR , A DIV. OF BOSTON SCIENTIFIC CORP·Product code DQX·December 19, 2006

    SYNCHRO 14 GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code DQX·September 20, 2007

    SYNCHRO .014 GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP. / NEUROCASCULAR DIVISION·Product code DQX·August 16, 2007

    SYNCHRO .014 GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP. / NEUROVASCULAR DIV.·Product code DQX·August 16, 2007

    SYNCHRO -14 NEURO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIVISION·Product code DQX·November 30, 2006

    SYNCHRO-14 NEURO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQX·September 12, 2007

    SYNCHRO GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQX·October 16, 2009

    SUPERTORQUE 5F MARKER BAND FLUSH CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DQO·March 27, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·March 18, 2011

    SI BRITE TIP UNKNOWN

    FDA Adverse Event
    CORDIS DE MEXICO·Product code DYB·March 28, 2008

    SYNCHRO 14 "S" NEURO GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code DQX·September 20, 2007