7 results
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17ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MERIDIAN HEMODIALYSIS MACHINE, MODEL 5M5576
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Vita Flex CR System with LLI
FDA 510(k)
FDA Class 2
·Radiology
EASYMAX V SELF MONITORING BLOOD GLUCOSE SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
NOTINGHM SHLDR HUM HEAD 48X17 OFFSET
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWS·January 19, 2016
HOYER PRESENCE
FDA Adverse Event
Injury
·APEX HEALTHCARE MFG INC.·Product code FNG·March 1, 2013
TERUMO PERFUSION SYSTEM 8000
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code JOR·February 4, 2011
REVEAL LINQ
FDA Adverse Event
Malfunction
·IPG MFG SWITZERLAND·Product code DSI·August 8, 2014