BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

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    ULTRABLATOR ELECTRODE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BACTON TM, BASIC TM, APO A-I REAGENT

    FDA 510(k)
    FDA Class 1 ·Immunology

    KINAMED ATH 22MM COCR TOTAL HLIP FEMORAL HEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·March 5, 2020

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·March 5, 2020

    ADJUST ADJUSTABLE SGL INCISION SLING

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON)·Product code PAH·March 1, 2013

    HUDSON LARGE VOLUME NEBULIZER

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CAF·January 12, 2011

    VIVA XT

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code NIK·August 8, 2014

    Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026