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

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    CONTOURED RAISED TOILET SEAT

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    GE LOGIQ 9, MODELS 2188900, 2375600, 2404587 AND 5150000

    FDA 510(k)
    FDA Class 2 ·Radiology

    PILLAR SA PTC

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ATTUNE MEDIAL DOME PAT 41MM

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code JWH·June 5, 2023

    UNKNOWN DEPUY TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code JWH·April 21, 2014

    ASR UNI FEMORAL IMPL SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·September 26, 2012

    XACT CAROTID STENT SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code NIM·July 15, 2010

    Reamer / Irrigator / Aspirator (RIA): RIA Drive Shafts, RIA Tube Assemblies, sterile, RIA Reamer Head, sterile (12.0mm-19.0mm); intended to clear the medullary canal of bone marrow and debris and to effectively size the medullary canal for the acceptance of an intramedullary implant or prosthesis

    FDA Enforcement
    Class II ·Terminated·Synthes, Inc.·July 22, 2015