BEUDAMED
    11 results · 30ms · Sources: EU EUDAMED, US FDA

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    Nexxt Matrixx System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EarQ

    FDA UDI
    Oticon A/S·05707131342348·G10, BTE 13 2.4G 85 C092 EARQ

    FU HONG INDUSTRIES LIMITED SOOTHER TEETHER

    FDA 510(k)
    FDA Class 2 ·Dental

    RT200

    FDA 510(k)
    FDA Class 2 ·Neurology

    COMP RVRS 25MM BSPLT HA+ADPTR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·March 8, 2021

    COBAS 600 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 7, 2008

    CLAMP F/ILIAC CONNECTOR F/FIXED-L

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code NKB·June 27, 2013

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·July 29, 2011

    FREESTYLE LIBRE 14 DAY

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE INC·Product code PZE·September 5, 2023

    FREE STYLE LIBRE 2

    FDA Adverse Event
    Injury ·ABBOTT DIABETES CARE INC.·Product code QLG·June 10, 2022

    Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020

    FDA Enforcement
    Class II ·Terminated·Cardinal Health 200, LLC·February 26, 2020