BEUDAMED
    6,811 results · 29ms · Sources: EU EUDAMED, US FDA

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    FDA UDI
    TELEFLEX INCORPORATED·00801902070142·Epidural Catheterization Kit with FlexTip Plus(...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·20801902070146·FlexTip Plus(R) Epidural Catheterization Kit

    SONDERANFERTIGUNG HKL

    FDA Adverse Event
    Malfunction ·MEDEX, INC.·Product code FMF·July 1, 2005

    SAVINA 300

    FDA Adverse Event
    Malfunction ·DRÄGERWERK AG & CO. KGAA·Product code CBK·May 6, 2021

    ALARIS GP PLUS

    FDA Adverse Event
    Injury ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·October 20, 2020

    ALARIS GP LVP DRUGS & DOSING

    FDA Adverse Event
    Injury ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·October 20, 2020

    CORO SET HKL, CHEMNITZ

    FDA Adverse Event
    Malfunction ·MEDEX·Product code FPA·April 7, 2005

    STRATOS LV-T

    FDA Adverse Event
    Injury ·BIOTORNIK SE & CO. KG·Product code NKE·February 7, 2012

    HKL SET REGIONAL SPITAL BIEL

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code DRS·December 2, 2008

    OPMI LUMERA 700

    FDA Adverse Event
    Injury ·CARL ZEISS MEDITEC AG (OBERKOCHEN)·Product code HRM·December 19, 2023

    8F ANGIO-SEAL STS PLUS VASCULAR CLOSURE DEVICE, OUS

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code MGB·February 25, 2020

    BD SYRINGE 10ML LL EUROGRAPHICS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 28, 2025

    OXF KNEE PH3 I/M ROD RMVL HK L HK

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LXH·April 28, 2022

    OXF KNEE PH3 I/M ROD RMVL HK L HK

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LXH·June 11, 2019

    OXF KNEE PH3 I/M ROD RMVL HK L HK

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LXH·June 21, 2019

    OXF KNEE PH3 I/M ROD RMVL HK L HK

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code HWT·March 30, 2020

    OXF KNEE PH3 I/M ROD RMVL HK L HK

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code NRA·November 11, 2019

    Retinoscope, Ac-Powered

    FDA classification
    FDA Class 2 ·Retinoscope, Ac-Powered

    HTL-STREFA, INC.

    FDA registration
    HTL-STREFA, INC.·7 products·🇺🇸 United States

    HTL-STREFA S.A.

    FDA registration
    HTL-STREFA S.A.·8 products·🇵🇱 Poland