BEUDAMED
    12 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Statera-C™ Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Kitazato ET Catheter

    FDA UDI
    KITAZATO CORPORATION·04580745042207·

    Tecomet

    FDA UDI
    TECOMET INC.·00841435120129·MINI-TIP RONGEUR 40D

    Non-contact Infrared Body Thermometer, Model HTD8808C, HTD8818A, HTD8816C

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Multifrax Laser System

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

    ALINITY I TOXO IGM REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·April 22, 2026

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 26, 2021

    ENDURANT

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·November 6, 2014

    AIRLIFE TRI-FLO

    FDA Adverse Event
    Malfunction ·CAREFUSION 211, INC.·Product code BSY·August 29, 2011

    OT ULTRAMINI METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 18, 2013

    ALINITY I TOXO IGM REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·June 2, 2025

    ALINITY I TOXO IGM REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LGD·September 11, 2025