BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    HAKIM PROGRAMMABLE VALVE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    ELECTRIC MOBILITY'S SPARKY

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    DYNAPULSE 200M

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROFILE BIABUT 4.0 -Ø5.5

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·February 24, 2026

    PWRD ECH FLEX 60MM 34CM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·February 22, 2013

    MANGNUM REUSABLE CORE BIOPSY INSTRUMENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·December 28, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·August 4, 2014