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

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    SPEED XL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Oticon

    FDA UDI
    Oticon A/S·05707131264527·RIA PRO, KIT 312 DIR R H BE

    Freedom Pedicle Screw System

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215027827·

    MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7 MM; MICRUS ASCENT OCCLUSION BALLOON CATHETER 6X9 MM; MICRUS SUMMIT OCCLUSIO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO SERAQUEST VCA IGM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    BD PHASEAL PROTECTOR P50J

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·June 17, 2021

    AMPLATZER AMULET

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code NGV·August 6, 2024

    VERCISE GENUS?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code PJS·November 17, 2025

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    AFFINITY BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code HDD·May 12, 2011

    HT COMMAND

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code DQX·October 1, 2014