BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    BALLOON DILATION CATHETER

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

    LIGHT SOURCE, ENDOSCOP, XENON ARC

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

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ALTRX NEUT 36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 26, 2014

    ACCENT DR RF

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·November 10, 2010

    AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM - ANTERIOR

    FDA Adverse Event
    Injury ·BARD SHANNON LIMITED·Product code FTL·December 28, 2012

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020