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

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    Azurion R3.1

    FDA 510(k)
    FDA Class 2 ·Radiology

    Bard® Temporary Pacing Electrode Catheter Needle / Cannula (Introducer)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GoLIF! Lumbar Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COGNIS HE IS-1/DF-1/IS-1

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code NIK·November 11, 2008

    SYNCHRON CX PRO CLINICAL SYSTEMS, MODEL CX9 PRO

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·September 19, 2011

    HIP

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code LPH·July 25, 2013

    LARGE HEXAGONAL SCREWDRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code HXX·July 25, 2016

    MENISCAL SUTURE SYSTEM

    FDA Adverse Event
    Malfunction ·S.B.M. SAS·Product code GAT·March 10, 2026

    TRUE METRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH INC·Product code NBW·January 17, 2023