BEUDAMED
    24 results · 21ms · Sources: EU EUDAMED, US FDA

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    VANGUARD REPROCESSED COMPRESSION GARMENT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Zirlux

    FDA UDI
    HENRY SCHEIN, INC.·H65890124030·Zirlux Shading Liquid - Effects, light pink , 30ml

    CERASMART®

    FDA UDI
    Gc America Inc.·14548161320115·CERASMART™ 270 12 Cerec A3 LT 5p Block

    CERASMART®

    FDA UDI
    Gc America Inc.·D0470124031·CERASMART 270 12 A3 LT CEREC 5p

    MINI TREK™

    FDA UDI
    ABBOTT VASCULAR INC.·08717648180880·MINI TREK™ II Coronary Dilatation Catheter 2.00...

    MINI TREK™

    FDA UDI
    ABBOTT VASCULAR INC.·08717648180866·MINI TREK™ II Coronary Dilatation Catheter 2.00...

    MINI TREK™

    FDA UDI
    ABBOTT VASCULAR INC.·08717648180897·MINI TREK™ II Coronary Dilatation Catheter 2.00...

    MINI TREK™

    FDA UDI
    ABBOTT VASCULAR INC.·08717648180873·MINI TREK™ II Coronary Dilatation Catheter 2.00...

    MASEL

    FDA UDI
    Ortho Organizers, Inc.·00190707053949·GeoShapes™ Electrik™ Elastics 1/4" (6.35 mm) He...

    MINI TREK™

    FDA UDI
    ABBOTT VASCULAR INC.·08717648180859·MINI TREK™ II Coronary Dilatation Catheter 2.00...

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918111902·Large Drape_76inx60in_43g SMS_non-sterile_48ea/cs

    PRESTIGE IQ BLOOD GLUCOSE TEST SYSTEM, MODEL 507400, 537600, 550600, 561700, 563700

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NOVOFINE 31 DISPOSABLE NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918158082·Large Drape_76inx60in_43g SMS_Handi-Bin_non-ste...

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V·Product code FPA·November 21, 2025

    IPC® STYLUS TRANSNASAL BUR

    FDA Adverse Event
    Death ·MEDTRONIC XOMED INC.·Product code ERL·February 4, 2015

    BD DISCARDIT¿ II SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·June 20, 2022

    PELORIS RAPID TISSUE PROCESSOR

    FDA Adverse Event
    Injury ·LEICA BIOSYSTEMS MELBOURNE·Product code IEO·March 14, 2013

    CONCERTO II CRT-D

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code NIK·March 9, 2011

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 15, 2014