BEUDAMED
    35 results · 22ms · Sources: EU EUDAMED, US FDA

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    SYNERGEYES PS HYBRID CONTACT LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Nova

    FDA UDI
    PURELIFE, LLC·D79010601021·Nova Nitrile Powder-Free, Small, Super-stretchy...

    “Paonan” Orthopedic Manual Surgical Instrument (Non-Sterile)

    FDA UDI
    Paonan Biotech Co.,Ltd.·04719878787017·Ratcheting T-Handle

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA UDI
    FX SOLUTIONS·03701037312667·RATCHET T-HANDLE / HUDSON

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·July 28, 2006

    SONIC MODEL SO-300

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    GLUCOSE (HEXOKINASE) LIQUID REAGENT, MODEL G518-150

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·August 24, 2006

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·July 27, 2007

    INGEVITY+

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NVN·November 6, 2024

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·July 28, 2006

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 12, 2025

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·June 23, 2006

    WATCHMAN FLX LAA CLOSURE DEVICE & DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·December 21, 2022

    PELVISOFT ACELLULAR COLLAGEN BIOMESH

    FDA Adverse Event
    Injury ·TISSUE SCIENCE LABS.·Product code FTM·April 11, 2013

    AUU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 11, 2008

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Death ·AV-TEMECULA-CT·Product code NIM·April 15, 2011

    GORE® CARDIOFORM SEPTAL OCCLUDER

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MLV·December 18, 2021

    GORE® CARDIOFORM ASD OCCLUDER

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MLV·December 22, 2021

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code GIS·September 8, 2006