BEUDAMED
    15 results · 20ms · Sources: EU EUDAMED, US FDA

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    Matrix Pre-Treatment Controller

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    POWDER FREE NATURAL RUBBER LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DYNASTY ACETABULAR SHELL AND COCR ACETABULAR LINER

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    Zavation

    FDA UDI
    Zavation LLC·00842166123274·Cage - 16x18mm, 44-76mm, 15°

    Zavation

    FDA UDI
    Zavation LLC·00842166123267·Cage - 16x18mm, 44-76mm, 10°

    Zavation

    FDA UDI
    Zavation LLC·00842166123243·Cage - 16x18mm, 44-76mm, 0°

    Zavation

    FDA UDI
    Zavation LLC·00842166123250·Cage - 16x18mm, 44-76mm, 5°

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 24, 2025

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929066058·Corpectomy, 16Dx18Wx44H 0°

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929037034·Corpectomy, 16Dx18Wx44H 6°

    IMF SCREW Ø2 L8 SST

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code DZL·June 11, 2013

    ENTERALITE INFINITY EFP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICE GROUP·Product code LZH·July 24, 2014

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·July 8, 2011

    BD LUER-LOCK¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code FMI·September 25, 2023

    BD LUER-LOCK¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code FMI·September 25, 2023