BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    ABBOTT TESTPACK PLUS H. PYLORI

    FDA 510(k)
    FDA Class 1 ·Microbiology

    SURSHIELD SAFETY I.V. CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MaxCap Ped and MaxCap Neo

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TELESCOPE, 10 MM, 0°, QUICK LOCK, AUTOCLAVABLE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·October 31, 2023

    TELESCOPE, 10 MM, 30°, HD, QUICK LOCK, AUTOCLAVABLE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code EWY·June 5, 2023

    NC QUANTUM APEX¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·February 28, 2013

    AFFINITY BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code HDD·January 13, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 5, 2014

    SURSHIELD PUR SAFETY I.V. CATHETER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION - KOFU·Product code FOZ·December 22, 2017

    STA-Flex SUBTALAR SCREW, 8 mm x 14 mm, REF 982362, Sterile, Biomet Sports Medicine, 56 East Bell Drive, Warsaw, IN. Used to reduce excessive rearfoot pronation by blocking forward and downward displacement of the Talus, resulting in improved rearfoot alignment and foot function.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code HWC·January 21, 2011