7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HELIOSEAL F
FDA 510(k)
FDA Class 2
·Dental
MITEK MICRO QUICKANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
METALLIC INTRAMEDULLARY NAIL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
DAFILON BLUE 4/0 (1.5) 45CM DS16
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code GAR·November 7, 2016
MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT
FDA Adverse Event
C.T.M. HOMECARE PRODUCT, INC·Product code INI·January 28, 2013
REFLEXION SPIRAL X, 7F, VAR, RADIUS CIR. MAP. CATH
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, AF DIV·Product code DRF·November 30, 2010
MICROFRANCE® INSTRUMENT
FDA Adverse Event
Malfunction
·XOMED MICROFRANCE MFG·Product code KAE·July 14, 2014