BEUDAMED
    22 results · 38ms · Sources: EU EUDAMED, US FDA

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    Materialise Glenoid Positioning System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 19, 2022

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017712·K-Wire, Double Ended, Trocar Point, Diameter Si...

    SUPPLY CABLE

    FDA UDI
    Aktormed GmbH·04260463840544·

    External Fixation

    FDA UDI
    Life Spine, Inc.·00190837023157·Straight Plate, 1 Hole

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 15, 2023

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·June 28, 2023

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·March 5, 2021

    V200 VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RIGHTEST BLOOD GLUCOSE MONITORING SYSTEM, MODEL GM310

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    V200 / ESPRIT

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 16, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 28, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 19, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·May 20, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 7, 2021

    V200 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·December 9, 2020

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 21, 2021

    XIENCE EXPEDITION SV

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR, INC·Product code NIQ·May 31, 2013

    EVIA DR-T

    FDA Adverse Event
    Death ·BIOTRONIK SE & CO. KG·Product code NVZ·July 13, 2011

    PULMONETIC

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 203/PULMONETIC SYSTEMS, INC·Product code CBK·September 17, 2008