BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Zimmer Biomet Universal Navigation System

    FDA 510(k)
    FDA Class 2 ·Neurology

    Pre-Finisher

    FDA UDI
    TP ORTHODONTICS INC·00192029042373·4 Bicuspid Extraction w/Seating Springs

    SPACELABS ELANCE VITAL SIGNS MONITORING SYSTEM AND CENTRAL MONITOR SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SLENDERTONE FLEX MAX, MODEL 517 US

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·December 30, 2025

    RSVR MMT-103A 10PK 3CC 13L STRL

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code FMF·October 2, 2008

    CVC KIT: 14 GA X 20 CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC·Product code DQY·June 21, 2013

    VITROS CHEMISTRY PRODUCTS VALP REAGENT

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code LEG·November 6, 2007

    BD BACTEC¿ MGIT¿ 960 SIRE KIT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·May 6, 2022

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·January 5, 2023

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·January 10, 2023

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·October 21, 2022