7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TSRH OPEN HEAD BONE SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
Epimed
FDA UDI
EPIMED INTERNATIONAL, INC·00818788021557·Stingray® Epidural Catheter Connector 19g
IBIS EXPLORER AND MARKUP SOFTWARE
FDA 510(k)
FDA Class 2
·Radiology
STRYKER TITANIUM CROSS-SCREW SYSTEM, MODEL 234-500-1XX
FDA 510(k)
FDA Class 2
·Orthopedic
TELIGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013
ACCU-CHEK SPIRIT COMBO
FDA Adverse Event
Injury
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·November 23, 2010
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·July 3, 2014