7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
TRUE DILATATION BALLOON VALVULOPLASTY CATHETER, 20MM X 4.5 CM, 22MM X 4.5CM, 24 MM X 4.5CM, 26MM X 4.5CM
FDA 510(k)
FDA Class 2
·Cardiovascular
APNEARX
FDA 510(k)
FDA Class 2
·Dental
FLOWMEDICA BIFURCATED INFUSION SYSTEM, INFUSION CATHETER AND INTRODUCER SHEATH
FDA 510(k)
FDA Class 2
·Cardiovascular
ALLURA XPER FD
FDA Adverse Event
Malfunction
·Product code IZI·April 22, 2021
LEVEEN? COACCESS?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code GEI·May 29, 2013
ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL CO.·Product code MTA·June 15, 2011
RESOLUTION CLIP DEVICE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MND·August 22, 2008