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

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    MEMFIX SCREWS

    FDA 510(k)
    FDA Class 2 ·Dental

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756352307·AVR WCI PACK

    Spunbond light blue round cap

    Device
    EU MDR · Eu Md Class 1 ·ALLE S.R.L.·On the market·29 countries

    PEDICLE SCREW 03.58.225 MUST MC SCREW Ø5X45 CANNULATED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·November 22, 2023

    FEMTEC LASER SYSTEM FOR CAPSULOTOMY

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    LORENZ FIDUCAIL SCREW

    FDA 510(k)
    FDA Class 2 ·Neurology

    M.U.S.T. MIDLINE CORTICAL (MC) SCREW SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·April 9, 2026

    M.U.S.T. MIDLINE CORTICAL (MC) SCREW SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·November 18, 2025

    M.U.S.T. MIDLINE CORTICAL (MC) SCREW SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·July 11, 2025

    MYSPINE

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code PQC·September 27, 2024

    BARDEX LUBRICATH FOLEY CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC.·Product code KOD·November 18, 2010

    INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·January 11, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 2, 2014

    PEDICLE SCREW MUST MC SCREW Ø6X45

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·December 21, 2022