BEUDAMED
    12 results · 29ms · Sources: EU EUDAMED, US FDA

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    VSP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Polystar HK

    FDA UDI
    Merz Dental GmbH·D7091984350·anteriors; shade B3; mould 93 S

    Masel

    FDA UDI
    Ortho Organizers, Inc.·00190707035488·.016 X .016 Lower Elastinol™ Natural Form Archw...

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111345210·MICRO FCP STR 6MM X.4MM 6 IN

    UNIREST COMPOSITE RESTORATIVE, SELF CURED

    FDA 510(k)
    FDA Class 2 ·Dental

    SALTER LABS MODEL #4009 SAMPLE LINES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CURRENT RF VR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·February 28, 2013

    FOXCROSS PTA CATHETER

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code LIT·February 10, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·August 6, 2014

    VERSA-DIAL/COMP TI STD TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·March 6, 2019

    VERSA-DIAL 42X18X46 HUM HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·March 6, 2019

    PT HYBRID GLEN POST REGENEREX

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·March 6, 2019