308 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MULTICHEM WBT
FDA 510(k)
FDA Class 1
·Clinical Toxicology
Reef TO
FDA UDI
Seaspine Orthopedics Corporation·10889981190705·Interbody, 11mm x 32mm x 17mm, 5 Deg
Reef TO
FDA UDI
Seaspine Orthopedics Corporation·10889981204853·Trial, 11mm x 32mm x 17mm, 5 Deg
WIDE 3MP GRAYSCALE TFT LCD MONITOR IF2103A
FDA 510(k)
FDA Class 2
·Radiology
ZOLL PROPAQ M
FDA 510(k)
FDA Class 2
·Cardiovascular
TOTAL ASR FEM IMP SIZE 55
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·May 29, 2013
60CC SYRINGE ONLY LUER LOCK TIP
FDA Adverse Event
Other
·COVIDIEN·Product code FMF·June 4, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 1, 2014
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
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·November 19, 1999
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