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

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    SUPERCATH5

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AGXO

    FDA UDI
    Oticon A/S·05707131270009·H160, DESIGNRITE 10 WL CBE AGXO

    FOERSTER HELLMAN CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896023864·FOERSTER-HELLMAN CLAMP DOUBLE ARTICULATING SHAFT

    DYNAGRAFT II

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    VENTED AUTOFEED CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·August 20, 2014

    VERCISE? CARTESIA?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code MHY·January 16, 2026

    FLEXTEND

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code DTB·October 3, 2014

    RECAP SHELL COCR PC 54/48MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·May 31, 2013

    ADJUSTABLE PIN COLLET

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code GET·June 17, 2011

    Micro Screen 6 Panel Cup with Adult (AU), Item No. MSCA-6MBAU

    FDA Enforcement
    Class III ·Terminated·Ameditech Inc·December 30, 2015

    GALAXY G3 XSFT HEL 2MM X 8CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·February 16, 2021