7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PICOALEX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Demetra Dermatoscope BDEM-01
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Catapult Guide Sheath
FDA 510(k)
FDA Class 2
·Cardiovascular
FREESTYLE AORTIC ROOT BIOPROSTHESIS
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code LWR·November 11, 2014
MOOG
FDA Adverse Event
Malfunction
·MOOG·Product code LZH·September 6, 2011
UNICEL® DXC 600I SYNCHRON® ACCESS CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code JJE·July 23, 2013
MENTOR SMOOTH ROUND MODERATE PROFILE
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FWM·January 7, 2020