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

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    Air Compression Therapy Device

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    DJO SURGICAL

    FDA UDI
    Encore Medical, L.P.·00190446838012·SPECIAL, EMPOWR REV KNEE MONOBLOCK TIBIAL TRAY ...

    HHM

    FDA UDI
    Oticon A/S·05707131357465·G300 SC, MINIRITE R LI-ION 2.4G C048 HHM

    CODMAN

    FDA UDI
    Cerenovus, Inc.·10886704066828·CODMAN SLIM-LINE Aneurysm Clip 45 Degree Angle ...

    NA

    FDA UDI
    Synthes GmbH·10886982142603·2.4MM CORTEX SCREW 3.5MM HEAD/SELF-TAPPING 48MM

    GUIDANT RETRIEVER DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CARDIOVENTION POWERBASE CONSOLE, MODEL PBC-100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD VACUTAINER® SST¿ TUBE 13X75MM, 3.5 ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 27, 2017

    NUROLON NYLON SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAR·October 24, 2018

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

    BD VACUTAINER® SST¿ TUBE 13X75MM, 3.5 ML. GOLD BD HEMOGARD¿ CLOSURE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 27, 2017

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code DTK·August 11, 2011

    TRABECULAR METAL PRESS-FIT FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code LPH·June 28, 2013

    IMPLANTABLE NEUROSTIMULATOR FOR SCS

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·November 10, 2016

    IMPLANTED SUBCORTICAL ELECTRICAL STIMULATOR (MOTOR DISORDERS)

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·October 12, 2016

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 27, 2016

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 27, 2016

    STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·May 11, 2016

    IMPLANTED SUBCORTICAL ELECTRICAL STIMULATOR (MOTOR DISORDERS)

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·October 12, 2016