6 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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WRIGHT PLASTER OF PARIS BONE VOID FILLER KIT (SUBJECT TO REVISION)
FDA 510(k)
FDA Class 2
·Orthopedic
VERIFY Incubator for Assert Self Contained Biological Indicators
FDA 510(k)
FDA Class 2
·General Hospital
XODUS MEDICAL ANTI-FOG SOLUTION
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HEARTSTART ONSITE
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 23, 2014
ECHELON*FLEX60
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·February 15, 2013
840 VENTILATOR
FDA Adverse Event
Malfunction
·PURITAN BENNETT CORP.·Product code CBK·December 20, 2010