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

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    CLEAR-IT ANTI-FOG, MODEL PS003

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

    FILLAUER, LLC

    FDA registration
    FILLAUER, LLC·22 products·🇺🇸 United States

    EQUITY

    FDA 510(k)
    FDA Class 2 ·Dental

    BIOPORTA G, MODEL 2052

    FDA 510(k)
    FDA Class 2 ·Dental

    ABG SYRINGE,1 ML LUER-LOK SYRINGE WITH NEEDLE. REGULAR PLUNGER STOPPER &TIP CAP.

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 7, 2017

    BD PRESET¿ SYRINGE WITH ATTACHED NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 6, 2017

    3 ML BD PRESET¿ SYRINGE WITH BD LUER-LOK¿ TIP. 22 G X 1 IN BD ECLIPSE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 4, 2017

    BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 7, 2018

    BD PRESET¿ SYRINGE WITH ATTACHED NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 27, 2017

    BD PRESET¿ SYRINGE WITH ATTACHED NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 7, 2017

    ITREL 3

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·March 27, 2013

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 17, 2011

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 28, 2008

    BD PRESET¿ SYRINGE WITH ATTACHED NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 27, 2017

    BD PRESET¿ ARTERIAL BLOOD COLLECTION SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 9, 2022

    BD PRESET¿ SYRINGE WITH ATTACHED NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·October 11, 2022

    SYR ABG PRESET 1(.6) S/T 23X1 CE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 24, 2019

    BD PRESET¿

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·January 13, 2022

    NEOBLUE LED PHOTOTHERAPY SYSTEM

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL INCORPORATED·Product code LBI·August 10, 2018

    CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026