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

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    Reveal LINQ Insertable Cardiac Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694019767·FPS 2.0mm x 8mm Standard Screw

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193100616·EVOS Straight HA PEEK, 8mm x 8mm x 22mm, Flat 5...

    ARKEO, Wedge Fixation System

    FDA UDI
    Auxano Medical LLC·00850055649774·ARKEO Evan's Wedge, 20x20x08

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694073707·FPS 2.0 x 8mm Screw Sterile Qty 5

    TOUCHPACS SUITE

    FDA 510(k)
    FDA Class 2 ·Radiology

    STS RANGE , MODELS STS20,STS30,STS40

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ETHIOCON

    FDA Adverse Event
    Malfunction ·Product code GCJ·February 9, 2009

    UNKNOWN MESH PRODUCT (EWHU)

    FDA Adverse Event
    Injury ·ETHICON INC·Product code FTL·August 15, 2011

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·October 29, 2014

    AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code FNL·July 8, 2013

    ENDO STITCH SURGIDAC DLU

    FDA Adverse Event
    Malfunction ·NORTH HAVEN - USS·Product code MFJ·May 21, 2008

    CRITICATH

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CRITICAL CARE SYSTEMS PTE LTD.·Product code DYG·May 21, 2008

    ENDOPATH DEXTRUS SEAL CAP ASSEMBLY WITH ACCESSORIES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GCJ·December 29, 2008

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·September 18, 2008

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALSON RESEARCH, LTD. / HUNTINGTON·Product code MFK·September 18, 2008

    ENDO CATCH II 15MM SPECIMEN POUCH

    FDA Adverse Event
    Malfunction ·SANTO DOMINGO - USS·Product code GCJ·March 24, 2008

    ACCU-CHEK D-TRON PLUS

    FDA Adverse Event
    Death ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·April 23, 2008

    MEDEFIL

    FDA Adverse Event
    Injury ·MEDEFIL·Product code NZW·May 23, 2008

    T-SLING

    FDA Adverse Event
    Injury ·HERNIAMESH SR1·Product code FTL·January 26, 2012