BEUDAMED
    23 results · 25ms · Sources: EU EUDAMED, US FDA

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    Vdrive system, Vdrive Duo, Vdrive with V-Sono

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04064984699540·GENUMEDI PSS BLUE SIZE II

    DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169524217·TRIAL 2150312 PLATE TRIAL 12MM

    HHM

    FDA UDI
    Oticon A/S·05707131287304·H110V2, MINIRITE 312 WL CBE HHM

    ECHO PRESS-FIT HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304467903·

    Echo® Press-Fit Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868261022·

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100066·TEMPORAL SPECULUM CLOSED WIRE

    Scorpio

    FDA UDI
    Howmedica Osteonics Corp.·07613154020096·Posterior Stabilized Tibial Insert

    BD SYRINGE 5ML LL BNS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·October 30, 2025

    SPACELABS HEALTHCARE

    FDA UDI
    SPACELABS HEALTHCARE (WASHINGTON), INC·10841522127342·SAMPLE LINE,AGENT,W/SAMPLING TEE,7',50/BX

    VITROS CHEMISTRY PRODUCTS IGA REAGENT

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code CFN·January 30, 2024

    AMIGO INSULIN PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DISTALOCK FEMORAL INTRAMEDULLARY NAIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    5-LEAD,ECG,UNIV,SNAP,36",INT'L

    FDA UDI
    Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904059204·

    VITROS 5600 INTEGRATED SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code JJE·March 31, 2023

    INTELLIVUE MULTI-MEASUREMENT MODULE X3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·June 12, 2025

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 7, 2014

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·May 30, 2013

    STERILIZATION CASE

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·June 7, 2011

    RADIFOCUS GLIDEWIRE V

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 6, 2015