7 results
·
25ms
·
Sources: EU EUDAMED, US FDA
SOLAR 9500 INFORMATION MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
247
FDA UDI
SUNTECH MEDICAL, INC.·10840935106593·
STERITITE UNIVERSAL CONTAINER SYSTEM AND MEDITRAY PRODUCTS
FDA 510(k)
FDA Class 2
·General Hospital
Vanguard XP Knee System
FDA 510(k)
FDA Class 2
·Orthopedic
S3 EX - 3005
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 5, 2013
REVEAL DX
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code DSI·February 15, 2011
CONCERTO II CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 7, 2014