BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    ACRY TEMP

    FDA 510(k)
    FDA Class 2 ·Dental

    NA

    FDA UDI
    Zimmer, Inc.·00889024132375·

    ClearPoint System

    FDA 510(k)
    FDA Class 2 ·Neurology

    MINI QUICKANCHOR AND QUICKANCHOR PLUS WITH ORTHOCORD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·April 24, 2014

    SEE H-10

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL COMPANY·Product code HQL·October 3, 2012

    COMMUNICATOR

    FDA Adverse Event
    Malfunction ·EXTERNAL MANUFACTURER·Product code LWS·July 27, 2010

    Philips Azurion 7M20 systems with FlexArm ceiling-mounted system, Interventional Fluoroscopic X-Ray System, Model Numbers 722079 and 722224

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·September 11, 2024