6 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
PISTON SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
STOMA BONE SCREW
FDA 510(k)
FDA Class 2
·Dental
FEATHER 01 02 03 04 (Model:01)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·February 9, 2013
GREENLIGHT HPS BPH FIBER OPTIC
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·July 23, 2014
PALMAZ GENESIS OPTA PRO
FDA Adverse Event
Injury
·CORDIS EUROPA, N.V.·Product code FGE·January 7, 2011