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

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    Filters Regulation: Us FDA ×

    Diode Laser Body Sculpture Systems

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

    Unity Total Knee System

    FDA UDI
    CORIN LTD·05056139232541·Patella Drill Guide Dome Sz 1 to 3

    Intrigue

    FDA UDI
    LANCER ORTHODONTICS, INC.·00817573021178·INTRG WHISP ROTH BIC HK-7T 0A 022 UR

    KLINIDRAPE SURGICAL DRAPES

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

    E.G. SCAN(TM) II ESOPHAGOSCOPE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    VIDAS® HCG

    FDA Adverse Event
    Injury ·BIOMERIEUX,SA·Product code JHI·June 17, 2019

    10 ML BD POSIFLUSH¿ NORMAL SALINE SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·November 19, 2021

    CD HORIZON

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code LXH·February 24, 2025

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·August 26, 2011

    CONV PN SEC MACRO OL

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·October 30, 2008

    NBCA LIQUID EMBOLIC KIT

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code KGG·July 17, 2013