BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    HEALIX ADVANCE Anchor with DYNACORD Suture

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MIO ADVANCE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code FPA·July 20, 2021

    WATCH-PAT200U (WP200U)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TBD

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL ¿ NEUROMODULATION·Product code GZB·October 10, 2014

    CANCELLOUSSCR Ø4 L30/14 TI

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·June 17, 2013

    INSIGNIA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 24, 2011

    THERMAGE CPT SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code GEI·November 12, 2020

    THERMAGE CPT SYSTEM TIP

    FDA Adverse Event
    Injury ·SOLTA MEDICAL INC·Product code GEI·November 30, 2022

    UNKNOWN

    FDA Adverse Event
    Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·February 20, 2025