4 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LIFETEC ELITE V1.0
FDA Adverse Event
Malfunction
·IT SYNERGISTICS, LLC·Product code MMH·July 29, 2016
RT300-S, MODEL FA100052; RT300-SP, MODEL FA100053
FDA 510(k)
FDA Class 2
·Neurology
VACUETTE BLOOD COLLECTION TUBE 3ML K2E K2EDTA
FDA Adverse Event
Malfunction
·GREINER BIO-ONE NA INC.·Product code JKA·November 2, 2020
ARIS TRANSOBTURATOR KIT
FDA Adverse Event
Injury
·COLOPLAST A/S·Product code OTN·September 9, 2021