BEUDAMED
    22 results · 26ms · Sources: EU EUDAMED, US FDA

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    MEDIA CULTURE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Resectoscopy sheath

    FDA UDI
    SOPRO-COMEG GmbH·04059082031408·

    Resectoscopy sheath

    FDA UDI
    SOPRO-COMEG GmbH·04059082031743·

    FloShield/Plus

    FDA UDI
    MINIMALLY INVASIVE DEVICES, INC.·00815128020751·The FloShield/Plus System is a single-use, disp...

    Implant-One

    FDA UDI
    Implant Logistics, Inc.·D762APT0405300·Abutment, 400 Series Angled Post .5mm Cuff Heig...

    CONTINUOUS GLUCOSE MONITOR

    FDA Adverse Event
    Malfunction ·Product code QBJ·April 20, 2022

    BELLEGLASS HP ENAMEL

    FDA 510(k)
    FDA Class 2 ·Dental

    GEO STRUCTURE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    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

    HT70 VENTILATOR

    FDA Adverse Event
    Malfunction ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·April 3, 2013

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·March 18, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·May 9, 2008

    ARCOS TAPER ADAPTOR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·April 17, 2018