364 results
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TITAN GUIDEWIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
Mini-Mono®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70604541·Mini-Mono-Brackets Alexander 'S' .018" 400 Brac...
KIMTECH PURPLE NITRILE-XTRA EXAM GLOVES (XL)
FDA UDI
KIMBERLY-CLARK GLOBAL SALES, LLC·00036016506045·Examination Gloves
KIMTECH PURPLE NITRILE-XTRA EXAM GLOVES (XL)
FDA UDI
KIMBERLY-CLARK GLOBAL SALES, LLC·00036000506044·Examination Gloves
Kalitec Universal Instruments
FDA UDI
Kalitec Direct LLC·B07301K0604500·Tray, Base, 4.5"
DIMEX 2
FDA 510(k)
FDA Class 2
·Dental
THE ALBERTA LENS SM2, SULFOCON B
FDA 510(k)
FDA Class 2
·Ophthalmic
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 10, 2013
AU400 CLINICAL CHEMISTRY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER MISHIMA K.K.·Product code JJE·April 18, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·ANIMAS CORP.·Product code LZG·June 13, 2008
NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 16, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 3, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 23, 2026