BEUDAMED
    77 results · 24ms · Sources: EU EUDAMED, US FDA

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    Magicore II System

    FDA 510(k)
    FDA Class 2 ·Dental

    CODMAN

    FDA UDI
    Cerenovus, Inc.·10886704001324·CODMAN SLIM-LINE Aneurysm Clip Curved Blade Len...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694091589·1.6mm Driver Stem, Medium, Manual

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383512558·"An absorbent paper points is an endodontic pap...

    DARDIK CAROTID SHUNT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FIXED BEARING UNI COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER, WITH CARDIAC RESYNCHRONIZATIO

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code NIK·August 12, 2023

    MYLA V3.X CA

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code JQP·September 19, 2016

    PERMANENT PACEMAKER ELECTRODE

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code DTB·February 5, 2026

    PERMANENT PACEMAKER ELECTRODE

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code DTB·February 5, 2026

    UNIDRIVE GYN MORCELLATOR MOTOR SYSTEM

    FDA Adverse Event
    Injury ·KARL STORZ GMBH & CO. KG TUTTLINGEN, GERMANY·Product code GCJ·March 29, 2016

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 14, 2016

    ARCHITECT SHBG

    FDA Adverse Event
    Malfunction ·ABBOTT GERMANY·Product code CDZ·May 8, 2017

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·July 27, 2016

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·June 8, 2016

    IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT)

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL / ST. JUDE·Product code LWS·May 28, 2024

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·August 11, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014

    BURRS

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW MANSFIELD MANUFACTURING SITE·Product code HAB·July 2, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·October 19, 2016