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

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    MODIFICATION TO:ZILVER 518 BILIARY STENT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ZILVER 518 BILIARY SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 21, 2017

    ZILVER 518 SELF-EXPANDING STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 26, 2012

    Mini-Dalbo®

    FDA UDI
    Cendres+Métaux SA·07640166513834·Mini-Dalbo® Matrize E 083.01.2 0054

    CT LUCIA

    FDA UDI
    CARL ZEISS MEDITEC PRODUCTION, LLC·00843045101192·3-piece, monofocal, hydrophobic, acrylic, intra...

    AESCULAP - MIETHKE SHUNT SYSTEM W/ NPH-DSV

    FDA 510(k)
    FDA Class 2 ·Neurology

    MASTERSCREEN CPX AND OXYCON CPX

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·April 10, 2013

    ADAPTA DR

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·April 12, 2011

    ATLAS II VR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008

    INCLUSIVE TAPERED IMPLANT 4.2 MMD X 8 MML X 3.5 MMP

    FDA Adverse Event
    Malfunction ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·March 14, 2020

    INCLUSIVE TAPERED IMPLANT 4.2 MMD X 8 MML X 3.5 MMP

    FDA Adverse Event
    Malfunction ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·February 11, 2020

    INCLUSIVE TAPERED IMPLANT 4.2 MMD X 8 MML X 3.5 MMP

    FDA Adverse Event
    Malfunction ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·March 13, 2020

    INCLUSIVE TAPERED IMPLANT 4.2 MMD X 8 MML X 3.5MMP

    FDA Adverse Event
    Malfunction ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·February 6, 2020

    INCLUSIVE TAPERED IMPLANT 3.2MMD X 10MML X 3.0MMP

    FDA Adverse Event
    Malfunction ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·February 20, 2020

    INCLUSIVE TAPERED IMPLANT 4.2 MMD X 8 MML X 3.5 MMP

    FDA Adverse Event
    Malfunction ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·February 5, 2020

    BD ANGIOCATH¿ IV CATHETER 20GA 1.88IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·December 27, 2019