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

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    Filters Regulation: Us FDA ×

    FEVER LINE AND FEVER LINE PLUS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BIO-MODULAR REVERSE SHOLDER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RIONET HEARING AID HB-32P

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    PERCLOSE PROGLIDE

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC·Product code MGB·June 19, 2014

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 7, 2015

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·November 9, 2010

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

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