182 results
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32ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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JAN MAO WHEELCHAIR, MODELS JMC612-FL318EPP AND JMC612-FL418EPP
FDA 510(k)
FDA Class 1
·Physical Medicine
ISSYS
FDA UDI
SPINAL ELEMENTS·00840916106942·Monoblock Cross Connector 18mm
VESCO
FDA UDI
XERIDIEM MEDICAL DEVICES, INC.·20813939024931·18 Fr - Gastrostomy Tube - Dual ENFit Port (Tri...
Gastrostomy Tube - Dual ENFit Port (Tri-Funnel)
FDA UDI
XERIDIEM MEDICAL DEVICES, INC.·00813939024937·Gastrostomy Tube - Dual ENFit Port (Tri-Funnel)...
LUDLOW GRADIENT EDGE ADULT & PEDIATRIC MULTIFUNCTIONAL ELECTRODES
FDA 510(k)
FDA Class 2
·Cardiovascular
NITRILE EXAM GLOVE, POWDER-FREE, COLOR BLUE
FDA 510(k)
FDA Class 1
·General Hospital
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
OUTLOOK 400ES
FDA Adverse Event
Malfunction
·B BRAUN·Product code FRN·February 3, 2012
BD PHOENIX¿ PMIC/ID-106
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·November 26, 2024
ASR UNI FEMORAL IMPL SIZE 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·April 16, 2013
ENDEAVOR SPRINT RX
FDA Adverse Event
Death
·MEDTRONIC CARDIO VASCULAR GALWAY·Product code NIQ·June 18, 2008
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·April 11, 2011