BEUDAMED
    237 results · 20ms · Sources: EU EUDAMED, US FDA

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    ACON ONE STEP PREGNANCY TEST STRIP (URINE)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CONSULT HCG TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code JHI·March 4, 2025

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993203·anteriors; shade B2; mould BM

    MOJAVE Expandable Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CARDIOBLATE BIPOLAR RADIOFREQUENCY SURGICAL ABLATION SYSTEM, MODELS 60831, 60832, 60841

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

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·March 7, 2013

    ADVANTA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·January 21, 2011

    VIRTUOSO II DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·August 8, 2014

    Olympus Thunderbeat, 5 mm, 45 cm Front-Actuated Grip

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code LFL·October 22, 2025

    Olympus Thunderbeat 5 mm, 10 cm, Inline Grip

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code LFL·October 22, 2025

    Olympus Thunderbeat, 5 mm, 45 cm, Pistol Grip

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code LFL·October 22, 2025

    Olympus Thunderbeat, 5mm, 35 cm, Pistol Grip

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code LFL·October 22, 2025

    Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code LFL·October 22, 2025

    Olympus Thunderbeat, 5 mm, 45 cm Inline Grip

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code LFL·October 22, 2025

    Olympus Thunderbeat, 5 mm, 20 cm, Inline Grip

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code LFL·October 22, 2025

    Olympus Thunderbeat, 5 mm, 35 cm, Inline Grip

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code LFL·October 22, 2025

    Olympus Thunderbeat 5 mm, 35 cm, Front-Actuated Grip

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code LFL·October 22, 2025

    Olympus Thunderbeat 5 mm, 45 cm, Front-Actuated Grip Type S

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code LFL·October 22, 2025

    Olympus Thunderbeat 5 mm, 20 cm, Front-Actuated Grip Type S

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code LFL·October 22, 2025

    Olympus Thunderbeat, 5 mm, 35 cm, Front-Actuated Grip Type S

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code LFL·October 22, 2025