BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·General Hospital

    HEMOCLIP TRADITIONAL LIGATING CLIPS, HEMOCLIP PLUS LIGATING CLIPS, HORIZON LIGTING CLIPS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MICROLIFE MODEL MT18E1-1 (V932-1) DIGITAL UNDERARM ELECTRONIC THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CERTAIN GOLD-TITE LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·June 9, 2025

    DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORPORATION·Product code KDI·November 6, 2014

    TOTALCARE BARIATRIC

    FDA Adverse Event
    Malfunction ·HILL-ROM INC·Product code FNL·July 19, 2011

    UNKNOWN DEPUY TIBIAL INSERT

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 18, 2013

    CERTAIN TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·June 9, 2025