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

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    HENKE SASS WOLF OF AMERICA ARTHROSCOPE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TruForm

    FDA UDI
    Rmo, Inc.·00885797100023·MN 1MOL BD KT STD NO/L R&L 176

    Conformis Hip System

    FDA UDI
    Conformis, Inc.·00850268007545·DRIVER, RIGID, 3.5MM HEX

    PORTRAIT FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTHES (USA) RESORBABLE TACK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962155844·PEEK, LONGITUDINAL BLUNT BLADE, 24MMX60MM WIDE

    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

    MESH, SURGICAL

    FDA Adverse Event
    Injury ·W. L. GORE AND ASSOCIATES, INC.·Product code FTM·August 12, 2023

    3.5MM CORTEX SCREW SELF-TAPPING 32MM

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·April 26, 2013

    LIGHTSPEED VCT

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS LLC·Product code JAK·April 22, 2011

    RELION 1CC INS SYR 31X5/16

    FDA Adverse Event
    Malfunction ·TYCO HEALTHCARE/KENDALL·Product code FMF·July 17, 2008

    RUNTHROUGH NS

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 24, 2018

    RUNTHROUGH NS

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 30, 2018