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

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    IO-DRIVE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993081·anteriors; shade A3; mould IS

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code HET·June 8, 2006

    POCKET BVM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Rheonix STI TriPlex Assay, Rheonix EncompassMDx Workstation (instrument and software), Rheonix Urine Specimen Collection Kit

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·June 18, 2024

    METRX SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·June 10, 2024

    PULSE GEN MODEL 105

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·March 7, 2013

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·February 8, 2011