7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OSTEOMED SBF SYSTEM (SBF)
FDA 510(k)
FDA Class 2
·Dental
iNSitu Total Hip System
FDA 510(k)
FDA Class 2
·Orthopedic
ORTHO DEVLOPMENT CERAMIC FEMORAL HEAD
FDA 510(k)
FDA Class 2
·Orthopedic
VITALITY 2
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013
MOVEEN NIGHT BAG 2000 ML, 140 CM
FDA Adverse Event
Injury
·COLOPLAST A/S·Product code FAQ·December 1, 2010
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FKX·July 3, 2014
VITEK® 2 AST-P656 TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LON·December 18, 2018