BEUDAMED
    24 results · 27ms · Sources: EU EUDAMED, US FDA

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    LW UCLA Abutment

    FDA 510(k)
    FDA Class 2 ·Dental

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950025404·6' DISS FEMALE TO OHIO MALE NITROUS OXIDE HOSE ...

    Proxis™ Ureteral Access Sheath

    FDA UDI
    C. R. Bard, Inc.·00801741101717·Proxis™ Ureteral Access Sheath

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694021869·FPS 3.5mm Clearance Drill Bit

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694076500·FPS 3.5 Clearance Drill Bit Sterile Qty 2

    CIRCUL8 Luxe DVT Prevention Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Arthrex MaxForce MTP Compression Plates and Screws

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·January 28, 2014

    ILET BIONIC PANCREAS

    FDA Adverse Event
    Malfunction ·BETA BIONICS, INC.·Product code QFG·May 5, 2026

    CLICKFINE 32GX4MM DONGBAO 7ER

    FDA Adverse Event
    Malfunction ·YPSOMED AG·Product code FMI·June 8, 2024

    INTERSTIM

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·November 13, 2008

    SECURE ACUTE CARE BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·July 18, 2011

    LOCKSCR Ø5 SELF-TAP L85 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code KTT·July 17, 2013

    AORTIC EXCLUDER AAA ENDOPROSTHESIS (C3)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·April 1, 2019

    AORTIC EXCLUDER AAA ENDOPROSTHESIS (C3)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·March 12, 2019

    UNSPECIFIED BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·October 15, 2025

    BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE 5MG/4MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·May 23, 2024

    MEDTRONIC LEAD

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·January 14, 2025

    UNKNOWN CODMAN EVD CATHETER

    FDA Adverse Event
    Injury ·Product code JXG·May 30, 2017

    TRUE METRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·January 25, 2023