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

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    SOLUTION ADMINISTRATION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Duo™ Lumbar Interbody Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPY ANALYSIS TOOLKIT, MODEL SA9000

    FDA 510(k)
    FDA Class 2 ·Radiology

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·February 27, 2013

    TEMPERATURE PROBE

    FDA Adverse Event
    CINCINNATI SUB-ZERO PRODUCTS, INC.·Product code FLL·January 17, 2011

    ATTUNE PS FB INSRT SZ 3 6MM

    FDA Adverse Event
    Injury ·1219655 DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDIC·Product code JWH·August 5, 2014

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·January 22, 2024

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·January 22, 2024

    ARCHITECT C16000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·May 10, 2019