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

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    Volta AF-Xplorer

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TIBIAL NAIL, STANDARD T2 TIBIA 9X300 MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 12, 2012

    EPAD

    FDA 510(k)
    FDA Class 2 ·Neurology

    DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAM GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    GII C/R ART INS SZ 7-8 9MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·February 19, 2019

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·September 11, 2014

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code KWP·September 2, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 18, 2013