7 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE
FDA 510(k)
FDA Class 2
·Cardiovascular
Micro cup forceps, tubular model
FDA UDI
Spiggle & Theis Medizintechnik GmbH·04250381885581·straight, 2.5 mm, 20 cm
irriga...
IN VITRO DIAGNOSTIC REGEANT SET,CHOLINESTERASE
FDA 510(k)
FDA Class 1
·Clinical Toxicology
SCIMED CARDIOTHERM CARDIOPLEGIA DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 13, 2013
SYNCHRON® CX5 DELTA CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJC·February 16, 2011
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 8, 2014