194 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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BIO-INTRAFIX TIBIAL SCREW AND SHEATH
FDA 510(k)
FDA Class 2
·Orthopedic
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·H65810321671·ZODIAC GLOVE PF LATEX
ZODIAC
FDA UDI
HENRY SCHEIN, INC.·00304040056936·ZODIAC Medium
Baltic Denture System BD Load
FDA UDI
Merz Dental GmbH·D7091032167·Baltic Denture System BDLoad ↓ Mw7 PLSEum2DFm A...
KARMAN WHEELCHAIR
FDA 510(k)
FDA Class 1
·Physical Medicine
MODEL TOP END TERMINATOR TITANIUM MANUAL WHEELCHAIR
FDA 510(k)
FDA Class 1
·Physical Medicine
ENDOPATH XCEL
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY·Product code GCJ·March 13, 2013
ICON 25 HCG
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JHI·March 29, 2011
TERUMO STERNAL SAW
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWH·April 21, 2008
BD PHOENIX¿ NMIC-311
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026
BD PHOENIX¿ NMIC-311
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026
BD PHOENIX¿ NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 28, 2026
BD PHOENIX¿ NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 14, 2026
BD PHOENIX¿ NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 3, 2026
BD PHOENIX¿ NMIC-306
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·May 27, 2026
BD PHOENIX¿ NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 20, 2026
BD PANEL PHOENIX NMIC-311
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·August 18, 2024
BD PHOENIX¿ NMIC-306
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 1, 2026
BD PANEL PHOENIX NMIC-311
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 2, 2024