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

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    COMPOSITE RESTORATIVE MATERIAL/RADIOPAQUE

    FDA 510(k)
    FDA Class 2 ·Dental

    SwishPlant® Implant

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307105954·4.8mmD x 12mmL, 4.8mmD Platform

    Stern Snap® Drill & Tap Attachment

    FDA UDI
    STERNGOLD DENTAL LLC·00841549113840·Retrievable Drill & Tap option for removable re...

    Swish™ Healing Collar

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307116141·

    MEDICAM ARTHROSCOPE SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELECTROPROBE SINGLE-USE SURGICAL PROBE

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

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·January 9, 2013

    COULTER® LH 500 INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·November 22, 2010

    INSIGNIA

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 1, 2014