6 results
·
18ms
·
Sources: EU EUDAMED, US FDA
TRI-BALL
FDA 510(k)
FDA Class 2
·Anesthesiology
VITREORETINAL INFUSION CANNULA
FDA 510(k)
FDA Class 1
·Ophthalmic
CO2 SURGICAL LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MERIDIAN FILTER SYSTEM - FEMORAL
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·February 27, 2013
UNICEL® DXI 800 ACCESS® IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code DHA·February 16, 2011
REVEAL LINQ
FDA Adverse Event
Malfunction
·IPG MFG SWITZERLAND·Product code DSI·August 8, 2014