BEUDAMED
    11 results · 26ms · Sources: EU EUDAMED, US FDA

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    INJECT-SNARE

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

    ID-RING

    FDA UDI
    DiaDent Group International·08806383525633·Used for color coding files

    PENTAX Medical Video Colonoscope (EC38-i20cWL)

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

    BEAMCATH

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

    PREMIER ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWQ·August 12, 2011

    PREMIER® ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·March 3, 2017

    PREMIER® ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 3, 2017

    PREMIER® ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 7, 2015

    PMO COMBINED PROBE CONTAINING BOTH OXYGEN AND TE

    FDA Adverse Event
    Malfunction ·GMS·Product code DRF·November 11, 2010

    OXIMAX N-560 PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·MEDIANA·Product code DQA·March 4, 2014

    DEXTRUS 4136

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·December 27, 2012