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

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    Route 92 Medical Sheath System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Compression Staple System

    FDA UDI
    TORNIER, INC.·00846832058792·Staple

    DENTAL HANDPIECES, MODELS: KARAM STD/MINI; BREEZE STD/MINI: KARAM 45; DEXOR 45; KARAM 4H COUPLING

    FDA 510(k)
    FDA Class 1 ·Dental

    ANY PLUS SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNSPECIFIED BD INFUSION SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·December 15, 2022

    FUJIFILM DUODENOSCOPE MODEL ED-580T

    FDA Adverse Event
    Injury ·FUJIFILM CORPORATION·Product code FDT·September 5, 2023

    FUJIFILM ENDOSCOPE

    FDA Adverse Event
    Malfunction ·FUJIFILM CORPORATION·Product code FDS·March 18, 2022

    FUJIFILM DUODENOSCOPE ED-580T

    FDA Adverse Event
    Injury ·FUJIFILM CORPORATION·Product code FDT·March 5, 2025

    ACCENT SR RF OUS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 13, 2014

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·July 28, 2011

    INTRALASE FS2

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·June 26, 2013