BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    DU PONT XENOLITE(TM) RADIATION PROTECTION APPAREL

    FDA 510(k)
    FDA Class 1 ·Radiology

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TITAN

    FDA Adverse Event
    Malfunction ·COLOPLAST MANUFACTURING US, LLC·Product code FHW·May 29, 2014

    QUICK FLEX LV LEAD

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

    MBT CEM KEEL TIB TRAY SZ2.5

    FDA Adverse Event
    Injury ·DEPUY IRELAND ¿ REG. # 9616671·Product code NJL·January 4, 2013

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

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