7 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MODIFIED AML + ACETABULAR CUP PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
N/A
FDA UDI
Smith & Nephew, Inc.·00885556601235·MTO OBTURATOR BLUNT 3.5MM
MICROPLEX COIL SYSTEM-COSMOS
FDA 510(k)
FDA Class 2
·Neurology
STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
COULTER LH 780 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·June 27, 2014
MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·January 2, 2013
CENTURY BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·November 9, 2010