370 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SMARTTROAE
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
WY'EAST MEDICAL CORP.
FDA registration
WY'EAST MEDICAL CORP.·4 products·🇺🇸 United States
CEFOTAXIME
FDA 510(k)
FDA Class 2
·Microbiology
RHODIA BITE REGISTRATION MATERIAL
FDA 510(k)
FDA Class 2
·Dental
3023859-2005-00001
FDA Adverse Event
Product code FSA·June 7, 2005
TRIATHLON PS FEM COMPONENT, CEMENTED
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·March 27, 2013
4.0MM TI CORTEX EXPANSIONHEAD SCREW SELF-TAPPING 14MM
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code KWQ·March 14, 2011
ARCHITECT BENZODIAZEPINE
FDA Adverse Event
Other
·ABBOTT MANUFACTURING, INC.·Product code JXM·April 1, 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
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 20, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 9, 2025