6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HYBRID RESIN COMPOSITE
FDA 510(k)
FDA Class 2
·Dental
QWIK-1(TM) IN-LINE IV FLUID WARMER
FDA 510(k)
FDA Class 2
·General Hospital
285CI INFUSION PUMP, MODIFICATION
FDA 510(k)
FDA Class 2
·General Hospital
CAPSURE Z NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·February 15, 2013
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·December 23, 2010
SURGIPRO 6 X 6 MONOFILAMENT MESH
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY US SURGICAL·Product code FTL·July 17, 2014