6 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Solitaire Platinum Revascularization Device
FDA 510(k)
FDA Class 2
·Cardiovascular
SDI CA480 CLINICAL CHEMISTRY SYSTEM; SATURNO 300 CLINICAL CHEMISTRY SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
XPERT MRSA/SA BC (BLOOD CULTURE) ASSAY MODEL GXMRSA/SA-BC-10
FDA 510(k)
FDA Class 2
·Microbiology
GYNECARE TVT-AA ABDOMINAL
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·June 11, 2013
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·July 24, 2014
UNICEL DXC 800 PRO SYNCHRON SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code JJE·October 20, 2015