7 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OPHTA SIL {SELF-THREADING MONOKA (RITLENG TYPE)}
FDA 510(k)
FDA Unclassified
·Unknown
Cardiologs Holter Platform
FDA 510(k)
FDA Class 2
·Cardiovascular
LaparoVue
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DASHER -14 STEERABLE GUIDEWIRE
FDA Adverse Event
Injury
·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORP·Product code DQX·January 9, 2007
PELORIS RAPID TISSUE PROCESSOR
FDA Adverse Event
Injury
·LEICA BIOSYSTEMS MELBOURNE·Product code IEO·February 5, 2013
LIVIAN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 6, 2011
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
FDA Adverse Event
Injury
·TANDEM DIABETES CARE INC.·Product code LZG·July 11, 2014