BEUDAMED
    176 results · 26ms · Sources: EU EUDAMED, US FDA

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    VS-800 VITAL SIGNS MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Mini-Mono®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70602811·Mini-Mono-Brackets Alexander 'S' .018" 1000 Bra...

    Bengolea artery clamp

    FDA UDI
    Spiggle & Theis Medizintechnik GmbH·04250676732811·curved, anatomical, fine 21.5 cm

    WALLSTENT ENTERNAL PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEROX BIPOLAR HIGH IMPEDANCE LEAD MODELS: MEX 53/13-BP; 60/15-BP; 45-JBP; 53-JBP

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    BD PHOENIX PMIC110

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·October 19, 2021

    BD PHOENIX¿ M50 AUTOMATED MICROBIOLOGY SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·August 23, 2021

    BD PHOENIX PANEL PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 10, 2023

    BD PHOENIX PANEL PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 10, 2023

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·September 2, 2025

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·September 2, 2025

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·April 15, 2024

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 23, 2024

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 26, 2024

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 26, 2024

    HEARTSTART ONSITE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 11, 2013

    ONE TOUCH ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·June 10, 2008

    REVEAL XT

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DSI·April 15, 2011

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 27, 2024

    BD PHOENIX¿ PMIC/ID-106

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·August 26, 2024