9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VYGON DOUBLE LUMEN UMBILICAL CATHETER
FDA 510(k)
FDA Class 2
·General Hospital
UMBILICAL CATHETER
FDA Adverse Event
Malfunction
·VYGON·Product code FOS·February 17, 2021
Polystar Selection EDITION
FDA UDI
Merz Dental GmbH·D7091981630·anteriors; shade D2 light; mould BS2
Revolution External Plating System
FDA 510(k)
FDA Class 2
·Orthopedic
MAMMO WORKSTATION
FDA 510(k)
FDA Class 2
·Radiology
ENDOPATH DISPOSABLE SURGICAL TROCAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GCJ·April 3, 1998
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·February 27, 2013
TERUMO VIRTUOSAPH VEIN HARVESTING SYSTEM
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GCJ·January 31, 2011
3MM DIAMOND BALL, 15CM
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBE·December 18, 2013