BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    CMS RECORD AND VERIFY

    FDA 510(k)
    FDA Class 2 ·Radiology

    ESOP HA FEMORAL STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DOPPLEX ABILITY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MENTOR SMOOTH ROUND MODERATE PLUS PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·May 24, 2019

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 17, 2013

    ADAPTA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NVZ·December 13, 2010

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 9, 2014