195 results
·
43ms
·
Sources: EU EUDAMED, US FDA
EXPORT ASPIRATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
PERMITE
FDA UDI
SDI LIMITED·09336472001186·PERMITE 3SP REG 500
PERMITE
FDA UDI
SDI LIMITED·DO3640233032·
36M - Kentucky Utilities
FDA UDI
Certified Safety Manufacturing, Inc.·00766588233031·Kentucky Utilities - 36 Metal
Oscar 2, Model 250D
FDA UDI
SUNTECH MEDICAL, INC.·10840935108450·
IM-5B MICROINJECTOR
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CLEANTEXX POWDERFREE SYNTHETIC LATEX EXAMINATION GLOVE MADE WITH BARRIER-PRO BUTADIENE CO-POLMER
FDA 510(k)
FDA Class 1
·General Hospital
CENTRA BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·February 28, 2013
HYDRELLE
FDA Adverse Event
Injury
·ANIKA THERAPEUTICS, INC·Product code MOZ·March 14, 2011
ONE TOUCH ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·April 1, 2008
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
Hearing aid
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·audifon GmbH & Co. KG·1 device