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

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    CONQUEST SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014607368·SKYTRON 3600 3" STANDARD

    NA

    FDA UDI
    STRYKER CORPORATION·07613327056648·Sliding-Lock Atraumatic Grasper, Double Action.

    STRYKER LAPAROSCOPIC ATRAUMATIC GRASPER

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER GMBH & CO. KG·Product code GEN·January 9, 2025

    MEMCATH UROLOGY INTRODUCER SHEATH, MODEL 201

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LIFEPORT VTX ACCESS SYSTEM,MODEL VTX 7000 SERIES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 7, 2025

    ITOTAL G2

    FDA Adverse Event
    Malfunction ·CONFORMIS·Product code JWH·April 9, 2013

    OT ULTRAMINI METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·May 6, 2011

    PROLIEVE THERMODILATATION KIT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·July 23, 2008