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

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    REUTER BOBBIN VENTILA. TUBE-TITANIUM

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    PressON™

    FDA UDI
    NEXUS SPINE, L.L.C.·B6788203620·Rivet Removal Shaft

    METAFIX FEMORAL STEM FOR HEMI-ARTHROPLASTY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    P.O.G.S. 3.3 PORTABLE OXYGEN GENERATOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BRASSLER USA ORTHOPAEDIC PIN

    FDA Adverse Event
    Malfunction ·BRASSELER USA, MEDICAL L.L.C.·Product code HTY·March 10, 2014

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 6, 2012

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 5, 2015

    Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.

    FDA Enforcement
    Class II ·Terminated·STERILMED, INC.·December 16, 2015