BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    HEATWAVE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Natural Profile Healing Abutment 5.0mm x 1.0mm, RP, Ti

    FDA UDI
    STERNGOLD DENTAL LLC·00841549110726·Devices are used in dental implant applications...

    RASTRONICS CCI 10/3 HEARING AID ANALYSIS

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·November 22, 2010

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·January 9, 2013

    ENERGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014

    TO GORE-TEX® STRETCH VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021

    GORE-TEX® STRETCH VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021

    GORE-TEX® STRETCH VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DSY·July 27, 2021

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021