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

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    INTEGRAL HEMODIALYSIS CATHETER

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

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690199298·Patella Trial 26mm x 10mm

    OMNI Knee

    FDA UDI
    Omni Life Science, Inc.·00841690101901·All Poly 3 Peg Patella 26 mm x 10 mm

    TAPERLOC MICROP FMRL 5.0MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·November 30, 2018

    Mariner Outrigger

    FDA UDI
    Seaspine Orthopedics Corporation·10889981175481·Z-Rod, Dia. 5.5mm, Co-Cr, 260mm

    HANSATOME MICROKERATOME

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    GELBFISH FLEX VASCULAR DILATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    PARIETEX UGYTEX PP POSTERIOR KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·March 18, 2013

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·April 5, 2011

    LONG 45 ENDOCUTTER

    FDA Adverse Event
    Injury ·Product code GDW·April 28, 2008

    LOGIC CR TIB INSERT STD, SZ 6, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 30, 2025

    OPTETRAK LOGIC

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 1, 2024