BEUDAMED
    24 results · 25ms · Sources: EU EUDAMED, US FDA

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    PERIFUSE CATHETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    JOBST UltraSheer

    FDA UDI
    BSN MEDICAL, INC.·00035664215255·ULTRA SHEER 20-30 MM HG KNEE HIGH CLOSED TOE EX...

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167321215250·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167311215250·

    TOPCUT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PIONEER SPINOUS PROCESS FUSION PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·June 11, 2018

    ECHI GREENVILLE NC 2

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code DTZ·November 22, 2011

    ECHI GREENVILLE NC 2

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code DTZ·November 30, 2011

    AMIA AUTOMATED PD CYCLER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·December 15, 2020

    AMIA AUTOMATED PD CYCLER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·January 12, 2023

    STONYBROOK HSP NY NY 1

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code OEZ·September 15, 2015

    BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 6, 2017

    ENDURON 10D 54OD X 28ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS·Product code KWY·May 21, 2013

    PROTACK* 5MM INSTRUMENT

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY USSC PUERTO RICO INC·Product code GDW·September 26, 2014

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 13, 2011

    AMIA AUTOMATED PD CYCLER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·February 15, 2024

    C21785 IT TREVISO

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code GEI·December 14, 2012

    D731 MICRO 27 ARTERIAL FILTER WITH 27 MICRON PHISIO COATING

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTM·May 18, 2022

    D731 MICRO 27 ARTERIAL FILTER WITH 27 MICRON PHISIO COATING

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTM·March 17, 2022