6 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NEWPORT COMMUNICAT PROTOCOL INTERFACE ADAPTOR
FDA 510(k)
FDA Class 2
·Anesthesiology
DYNAPULSE 200M
FDA 510(k)
FDA Class 2
·Cardiovascular
MEDILASER-S MEL-444-S
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SQ-RX PULSE GENERATOR
FDA Adverse Event
Injury
·CAMERON HEALTH, INC.·Product code LWS·January 29, 2013
TERUMO ADVANCED PERFUSION SYSTEM 1
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·December 17, 2010
UNKNOWN_FRO_PRODUCT
FDA Adverse Event
Malfunction
·STRYKER LEIBINGER FREIBURG·Product code FRO·July 17, 2014