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

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    PULSE*SPRAY INFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Smith & Nephew TRUCLEAR ULTRA Mini Tissue Removal Device

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ARC SURGICAL BIOTRAK SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    GERISTORE

    FDA Adverse Event
    DENMAT HOLDINGS LLC·Product code EBG·February 7, 2013

    6.5CM ADULT CRANI ATTACHMT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·July 28, 2014

    EQUIPMENT MANAGEMENT SYSTEM

    FDA Adverse Event
    STERIS CORPORATION - MONTGOMERY·Product code FQO·January 14, 2011