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

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    TITANIUM INTRAMEDULLARY NAIL, TITANIUM LOCKING SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981529·anteriors; shade BL4; mould IL2

    Vanguard IEP Peripheral Balloon Angioplasty System with Integrated Embolic Protection

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SEPTAL BUTTON

    FDA 510(k)
    FDA Unclassified ·Unknown

    ASR ACETABULAR CUP 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 27, 2013

    ACUITY CENTRAL MONITORING

    FDA Adverse Event
    Malfunction ·WELCH ALLYN PROTOCOL, INC.·Product code DSI·January 12, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·August 5, 2014

    L.C. 5000/CE 2-CHANNEL PUMP (50/CASE)

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·August 22, 2013