7 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
INTIMAX THROMBECTOMY CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756997720·EMERGENCY C-SECTION PACK
LIGHTLAS 532 PHOTOCOAGULATOR
FDA 510(k)
FDA Class 2
·Ophthalmic
Aveta System
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
RESTORE ULTRA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 11, 2013
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·November 24, 2010
MITEK VAPR S90 4MM 90 DEGREE SUCTION ELECTRODE
FDA Adverse Event
Malfunction
·DEPUY MITEK·Product code GEI·July 2, 2014