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

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    Filters Regulation: Us FDA ×

    QUIDEL MOLECULAR DIRECT C. DIFFICILE ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SOLSTICE CROSS CONNECTOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    THERIRIDGE BLOCK, BONE GRAFT SUBSTITUTE

    FDA 510(k)
    FDA Class 2 ·Dental

    U-BLADE SET, TI GAMMA3 10.5X90MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·November 30, 2012

    BD VACUTAINER® PST¿ GEL AND LITHIUM HEPARINN (LH) BLOOD COLLECTION TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·October 21, 2021

    BD VACUTAINER® PST¿ GEL AND LITHIUM HEPARINN (LH) 65 UNITS BLOOD COLLECTION TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·December 8, 2021

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·May 17, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·September 27, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 14, 2011

    RS GLENOID PLATE R POST AUG, 8 DEG, RIGHT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·April 30, 2024