BEUDAMED
    79 results · 22ms · Sources: EU EUDAMED, US FDA

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    LIFESPAN EPTFE VASCULAR GRAFT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193113067·HA PEEK EVOS Straight, ,16mmx10mmx 30mm , FLAT ...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694003001·12 Hole Straight Plate

    Trestle Luxe

    FDA UDI
    ALPHATEC SPINE, INC.·00190376242361·Midline Hexalobe Temporary Fixation Pin

    NA

    FDA UDI
    STRYKER CORPORATION·04546540079343·4.0mm Pear

    NA

    FDA UDI
    STRYKER CORPORATION·04546540079350·5.0mm Pear

    NA

    FDA UDI
    STRYKER CORPORATION·04546540079367·6.0mm Pear

    AVITA SCANEO INFRARED EAR THERMOMETER, MODEL TS7

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TEOAE25

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ENTERPRISE2 4MMX23MM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code NJE·October 4, 2023

    NUCLEUS 24 CHANNEL HYBRID COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code PGQ·July 4, 2016

    NUCLEUS 24 CHANNEL HYBRID COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code PGQ·August 1, 2016

    Cochlear Implant With Combined Electrical Stimulation And Acoustic Amplification

    FDA Pre-Market Approval
    FDA Class 3 ·NUCLEUS HYBRID L24 COCHLEAR IMPLANT SYSTEM

    LYNX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·May 24, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·September 30, 2014

    ANEURX AAADVANTAGE STENT GRAFT SSYTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·June 10, 2011

    ENTERPRISE2 4MMX23MM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code NJE·January 22, 2024

    Cochlear Implant With Combined Electrical Stimulation And Acoustic Amplification

    FDA Pre-Market Approval
    FDA Class 3 ·Nucleus® Hybrid™ Implant System

    Cochlear Implant With Combined Electrical Stimulation And Acoustic Amplification

    FDA Pre-Market Approval
    FDA Class 3 ·NUCLEUS 24 HYBRID SYSTEM

    Cochlear Implant With Combined Electrical Stimulation And Acoustic Amplification

    FDA Pre-Market Approval
    FDA Class 3 ·Nucleus® Hybrid™ L24 Cochlear Implant System