6 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BLOOD PUMP MODEL 7000
FDA 510(k)
FDA Class 2
·Cardiovascular
PHADECODE DIFFERENTIAL FACTOR XA1 ASSAY
FDA 510(k)
FDA Class 2
·Hematology
GENTASAK
FDA 510(k)
FDA Class 2
·Clinical Toxicology
COULTER® ACT DIFF 2 ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·April 30, 2014
TELIGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 10, 2012
RIVAL PTA BALLOON DILATATION CATHETER
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·April 15, 2015