6 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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THERA-MIST(TM) NEBULIZER, MODEL 30000
FDA 510(k)
FDA Class 2
·Anesthesiology
HENNING MENISCAL SUTURE KIT
FDA 510(k)
FDA Class 1
·Orthopedic
ENSITE VELOCITY SYSTEM V1.3
FDA 510(k)
FDA Class 2
·Cardiovascular
SHILEY
FDA Adverse Event
Injury
·COVIDIEN·Product code JOH·June 9, 2014
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·November 2, 2010
LIGASURE ADVANCE PISTOL GRIP
FDA Adverse Event
Injury
·COVIDIEN LP·Product code GEI·December 18, 2012