10 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Arthrex Synergy UHD4 System
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169501942·INTERBODY 2153218 MEDIUM - 18 DEG 18MM
Portex
FDA UDI
ICU MEDICAL, INC.·00351688032495·
STERRAD CHEMICAL INDICATOR STRIP
FDA 510(k)
FDA Class 2
·General Hospital
DBX DEMINERALIZED BONE MATRIX PUTTY/PASTE/MIX
FDA 510(k)
FDA Class 2
·Orthopedic
SURESCAN
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 8, 2014
CAPSUREFIX
FDA Adverse Event
Injury
·MPRI·Product code DTB·June 8, 2013
PROTECTIVE SAFETY IV CATHETER
FDA Adverse Event
Malfunction
·SMITHS MEDICAL NORTH AMERICA·Product code FOZ·June 30, 2011
SYMBIQ 3.13 SINGLE C
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·December 10, 2012
A200 KNEE SYSTEM
FDA Adverse Event
Injury
·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code JWH·September 16, 2016