BEUDAMED
    16 results · 23ms · Sources: EU EUDAMED, US FDA

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    Ekso™ (version 1.1) and Ekso GT™ (version 1.2)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SMART USBLITE, MODEL M011120

    FDA 510(k)
    FDA Class 2 ·Neurology

    X12 STERILE REFLECTIVE MARKER SPHERE

    FDA 510(k)
    FDA Class 2 ·Neurology

    LINEAR? ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·July 30, 2025

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 24, 2025

    TAXUS (R) LIBERTÉ (R)

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 14, 2011

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 5, 2013

    MANUAL ORTHOPEDIC SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code LXH·September 10, 2008

    BIOMET SMOOTH KNEE STEM 14X80

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·June 9, 2017

    VANGUARD SSK 360 FEMUR R 67.5

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·June 9, 2017

    ABTHERA¿ NEGATIVE PRESSURE THERAPY UNIT

    FDA Adverse Event
    Injury ·KCI USA, INC.·Product code OMP·July 7, 2016

    BIOMET 360 OFFSET ADAPTER 2.5MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·June 9, 2017

    BIOMET SMOOTH KNEE STEM 12X40

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·June 9, 2017

    VANGUARD DA 360 TIBIAL BEARING ARCOM 63/67X18

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·June 9, 2017

    VANGUARD DA 360 O/S TIBIAL TRAY COCR 67

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·June 9, 2017

    NRG TRANSSEPTAL NEEDLE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DXF·October 15, 2015