BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    2000 SERIES PORTABLE RESUSCITATION SYST.

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707008385·STRAIGHT WIRES EXTRA SPRING HARD 19x25

    ARTHROCARE ELECTROSURGERY WANDS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Miha Bodytec II

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    OVERJET CARIES ASSIST

    FDA Adverse Event
    Malfunction ·OVERJET·Product code MYN·February 18, 2025

    TRANSSEPTAL NEEDLE, BRK SERIES, ADULT 18 GA, 71CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC. (AF-MINNETONKA)·Product code DRC·May 5, 2014

    CAPSURE SENSE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    VIBRANT SOUNDBRIDGE

    FDA Adverse Event
    Malfunction ·VIBRANT MED-EL HEARING TECHNOLOGY GMBH·Product code MPV·August 10, 2010