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

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    FMH RapidScreen

    FDA UDI
    IMMUCOR, INC.·10888234000907·The FMH RapidScreen kit is intended for use in ...

    OC-Auto

    FDA UDI
    POLYMEDCO CANCER DIAGNOSTIC PRODUCTS LLC·00816917024769·Personal Use Kit OC-Auto, for Frederick Memoria...

    Foam Headrest

    FDA UDI
    Southmedic Incorporated·10620974002366·Large Foam Headrest - Angled

    NA

    FDA UDI
    SOUTHERN IMPLANTS (PTY) LTD·06009544011149·Instrument, Fixture Mount Holder / I-WI Conve...

    iProven

    FDA UDI
    Sevenground Trading B.V.·08719699633230·FMH-139 is a One Step HCG Urine Pregnancy Test

    iProven

    FDA UDI
    Sevenground Trading B.V.·08719699633254·FMH-139 is a One Step HCG Urine Pregnancy Test

    iProvèn

    FDA UDI
    Masena Invest B.V.·08719481722029·Box with three midstream pregnancy tests

    iProven

    FDA UDI
    Sevenground Trading B.V.·08719699630901·FMH-139 is a One Step HCG Urine Pregnancy Test

    iProvèn

    FDA UDI
    Masena Invest B.V.·08719481722043·Box with five midstream pregnancy tests

    Foam Headrest

    FDA UDI
    Southmedic Incorporated·10620974002373·Small Foam Headrest - Angled

    FMH RAPIDSCREEN

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code LIM·September 4, 2014

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902117950·QuickFlash(R) Radial Artery Catheterization Kit...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·00801902043832·QuickFlash(R) Radial Artery Catheterization Kit...

    FMH RAPIDSCREEN

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code LIM·February 2, 2024

    BIOPINCE AUTOMATIC FULL CORE BIOPSY INSTRUMENT 18GX10CM

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES·Product code KNW·August 3, 2020

    BD VACUTAINER® SPECIALTY TUBES BD HEMOGARD¿/CLEAR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMH·December 7, 2017

    BD VACUTAINER® SST¿ BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·April 13, 2020

    BD PRESET¿ ARTERIAL BLOOD COLLECTION SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·January 10, 2020

    BD VACUTAINER® 9NC 0.109M PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·September 19, 2019

    BD VACUTAINER® SPECIALTY TUBES; DISCARD/NO ADDITIVE, HEMOGARD¿/ CLEAR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMH·December 14, 2017