BEUDAMED
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    ELEGANCE - DEO, MODIFICATION

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    YANTAI ATOMY DEO TECH DAILY-USE COMMODITY CO., LTD.

    FDA registration
    YANTAI ATOMY DEO TECH DAILY-USE COMMODITY CO., LTD.·1 product·🇨🇳 China

    INF SET CLEO 31" 9MM

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code FPA·February 7, 2022

    UNK

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·September 12, 2008

    INF SET CLEO 24" 9MM

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code FPA·May 23, 2023

    PALMAZ-SCHARTZ BALLOON -EXPANDABLE STENT W/DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·NEW JERSEY PLANT·Product code MAF·January 2, 1997

    EPICLL/ZOOM IN SERVICEVI DEO

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code HDD·January 17, 2013

    CASE-150ML SYRINGE W/HANDIFIL

    FDA Adverse Event
    Malfunction ·LIEBEL - FLARSHEIM CO.·Product code DXT·January 7, 2009

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·August 22, 2016

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·August 22, 2016

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·August 22, 2016

    INF SET CLEO

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·December 20, 2024

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·August 22, 2016

    INF SET CLEO 31" 9MM

    FDA Adverse Event
    Malfunction ·SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V.·Product code FPA·October 18, 2022

    IPC® HANDPIECE - XPS® STRAIGHTSHOT® M5

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·May 6, 2024

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 9, 2016

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP MMT-723RNAS

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·November 26, 2020

    UNKNOWN LIGASURE INSTRUMENT

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GEI·September 3, 2025

    CARDIOSAVE HYBRID W/ E/F PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 19, 2025

    ARROW-CLARK VECTORFLOW HEMODIALYSIS CATHETER

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code MSD·November 14, 2019