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

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    FORA GD20 BLOOD GLUCOSE MONITORING SYSTEM, U-RUGHT TD-4252D BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PULSE GEN MODEL UNKNOWN

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·April 24, 2026

    LEAD MODEL UNKNOWN

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·April 24, 2026

    PULSE GEN MODEL UNKNOWN

    FDA Adverse Event
    Injury ·LIVANOVA USA, INC.·Product code LYJ·April 24, 2026

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434571·Tasso+ convenience kit allows self-collection o...

    Novo Surgical Inc.

    FDA UDI
    NOVO SURGICAL, INC.·00842331171185·double-ended probe, stainless steel, 8" (20.0 cm)

    OrthoMedFlex

    FDA UDI
    ORTHOMEDFLEX LLC·M7161016310·Anterior Tray I

    Orthoquest

    FDA UDI
    Young Innovations, Inc.·00843471133866·T D-Form 014X025

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383502047·Gutta Percha Points is used to root canal filin...

    Young Specialties

    FDA UDI
    Young Innovations, Inc.·00840326426166·NiTi Thermal Archwire, D-Form .014x.025 10EA

    ALLURE® MB

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807101631041·ALLURE® MB SEW .018 LOWER 3

    CORTEX METAMAX

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AFFIITY CP CENTRIFUGAL BLOOD PUMP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN ENDO GIA SULU

    FDA Adverse Event
    Injury ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·January 6, 2022

    UNKNOWN ENDO GIA SULU

    FDA Adverse Event
    Death ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·January 7, 2022

    EN SNARE ENDOVASCULAR SNARE SYSTEM

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS INC·Product code MMX·May 3, 2013

    MAQUET MOBILE OPERATION ROOM TABLE ALPHAMAXX

    FDA Adverse Event
    Injury ·MAQUET GMBH·Product code FQO·August 27, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 11, 2011

    ACTIVA

    FDA Adverse Event
    Malfunction ·MPRI·Product code MHY·September 24, 2020

    ACTIVA

    FDA Adverse Event
    Malfunction ·MPRI·Product code MHY·September 24, 2020