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

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    Halyard Black-Fire Powder-Free Nitrile Exam Glove, Halyard Purple Powder-Free Nitrile Exam Glove

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777655·LUMBAMED BASIC DORSAL STAYS M SILVER III

    Ceramco® iC

    FDA UDI
    Dentsply International Inc.·D00142006330·CC-313

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540256973·SCREWDRIVER BLADE, 2.0MM SQUARE-FIT

    Olympus

    FDA UDI
    Gyrus ACMI, LLC·00821925047280·ES-IP iOR BWK Hamburg Hybrid (no rack)

    Apelo® / Apelo® MIS

    FDA UDI
    ATLAS SPINE, INC.·M68120063300000·T-Handle

    SYNTHETIC GLASS BONE GRAFT MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    NATURAL AND COLORED LATEX CONDOM WITH FLAVORS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    HEMOGLIDE KIT, PC-2

    FDA Adverse Event
    Malfunction ·C. R. BARD, INC. (BASD)·Product code MSD·December 12, 2008

    MICROLET®

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code QRL·April 23, 2026

    MICROLET®

    FDA Adverse Event
    Injury ·ASCENSIA DIABETES CARE US INC.·Product code QRL·April 3, 2025

    ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - CORK·Product code MCX·July 30, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 24, 2014

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·July 1, 2013

    MICROLET®

    FDA Adverse Event
    Malfunction ·ASCENSIA DIABETES CARE US INC.·Product code QRL·July 1, 2025

    MICROLET®

    FDA Adverse Event
    Injury ·ASCENSIA DIABETES CARE US INC.·Product code QRL·December 1, 2023

    INSPIRE 7F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code DTZ·September 15, 2022

    INSPIRE 7F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL.·Product code DTZ·March 12, 2024

    INSPIRE 7F

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·June 24, 2025