BEUDAMED
    13 results · 20ms · Sources: EU EUDAMED, US FDA

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    AUTOSPECT

    FDA 510(k)
    FDA Class 2 ·Radiology

    SW

    FDA UDI
    SW SAFETY SOLUTIONS INC.·00616489004035·PowerChem Neoprene Exam Gloves, Medium

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065661·INTRAORAL ELASTICS 2,5 oz 5/16" blue

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776384937·Chisel, bi-bevel, octagonal handle, 4mm tip, 7"...

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036029289·

    PRESTIGE IQ BLOOD GLUCOSE TEST SYSTEM, MODEL 507400, 537600, 550600, 561700, 563700

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MODIFICATION TO EBI XFIX DFS OPTIROM ELBOW FIXATOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·February 10, 2015

    3M TEGADERM ALGINATE AG SILVER DRESSING

    FDA Adverse Event
    Injury ·3M HEALTH CARE·Product code FRO·June 21, 2016

    ABSORB BIORESORBABLE VASCULAR SCAFFOLD SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·May 2, 2013

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·September 15, 2014

    CONCERTO II CRT-D

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code NIK·May 16, 2011

    Dermagraft, Human Fibroblast -Derived Dermal Substitute, 2 in. by 3 in..

    FDA Recall
    Terminated ·Smith and Nephew Wound Management (La Jolla)·Product code MGR·May 2, 2003