BEUDAMED
    14 results · 36ms · Sources: EU EUDAMED, US FDA

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    T-GEAR, MODEL TG/400-700

    FDA 510(k)
    FDA Class 2 ·Dental

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993224·anteriors; shade B2; mould UIL

    XPS® HANDPIECE - VISAO®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·December 9, 2015

    XPS® HANDPIECE - VISAO®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·January 8, 2016

    DENSICHECK PLUS

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Daytona® Small Stature Growth Rod Conversion Set

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    XPS HANDPIECE - VISAO

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·November 2, 2021

    DRILL 3334800 VISAO 80K HANDPIECE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code ERL·July 2, 2013

    XPS® HANDPIECE - VISAO®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ERL·December 1, 2017

    XPS® HANDPIECE - VISAO®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ERL·December 1, 2017

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·March 7, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 7, 2011

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014

    XPS® HANDPIECE - VISAO®

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·June 9, 2016