BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    TITERTEK AUTODROP

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ERA® Implant Abutment Micro Angled Base, 6mm Cuff (T)

    FDA UDI
    STERNGOLD DENTAL LLC·00841549104909·Implant retained overdentures are an establishe...

    VIDAS D-DIMER EXCLUSION II (DEX2)

    FDA 510(k)
    FDA Class 2 ·Hematology

    HELICAL COMPRESSION ANCHOR SYSTEM, CANNULATED SINGLE HELIX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEARTSTART XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 25, 2014

    REVEAL XT

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DSI·October 31, 2012

    ARCHITECT STAT TROPONIN-I

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code MMI·August 24, 2010

    MESH, SURGICAL, POLYMERIC

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·June 22, 2017

    MESH, SURGICAL, POLYMERIC

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·June 22, 2017

    MESH, SURGICAL, POLYMERIC

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·June 22, 2017

    MESH, SURGICAL, POLYMERIC

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·June 22, 2017

    MESH, SURGICAL, POLYMERIC

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·June 22, 2017