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

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    ReliaTack Articulating Reloadable Fixation Device with Deep Purchase Reloadable Tacks

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

    Medline

    FDA UDI
    MEDLINE INDUSTRIES, INC.·10889942140923·BIOPSY TRAY

    ProLift

    FDA UDI
    Life Spine, Inc.·00190837106249·Static Expandable Cage Trial, 10mm x 28mm x 10m...

    Best Medical International

    FDA UDI
    BEST MEDICAL INTERNATIONAL, INC.·00841365107238·

    SEMIAL SPINAL IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SUPERCROSS MICROCATHETER (130 CM), SUPERCROSS MICROCATHETER (150 CM) MODEL 5300, 5301

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code HAW·November 10, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·April 11, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·March 15, 2018

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code HAW·June 15, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 10, 2017

    DEXCOM G7 15 DAY CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·Product code QBJ·May 14, 2026

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·March 21, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 16, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 9, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·January 26, 2018

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·October 8, 2014

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 7, 2013

    COULTER LH 50 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·June 24, 2011

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 6, 2017