9 results
·
27ms
·
Sources: EU EUDAMED, US FDA
LIQUAEMIN SODIUM, HEPARIN SODIUM ETC.
FDA 510(k)
FDA Class 2
·Clinical Chemistry
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293319·
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690117940·Modular Tibia Inserter
CENTRIA T3 RIA
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CUTTER, P607 BONE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·April 24, 2014
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·October 4, 2012
TELIGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 27, 2010
On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement of diseased, damaged, or malfunctioning native or prosthetic heart valves in the aortic and mitral positions
FDA Enforcement
Class II
·Terminated·CryoLife, Inc.·July 19, 2017