6 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SFI-BAR
FDA 510(k)
FDA Class 2
·Dental
CODMAN CERTAS PROGRAMMABLE VALVE SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
POWER-FREE NITRILE PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·May 14, 2013
INSYNC SENTRY
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code NIK·June 16, 2011
SYNFIX(TM)-LR 30MM DEPTH/38MM WIDTH/15MM HEIGHT 8DEG-STER
FDA Adverse Event
Injury
·SYNTHES BETTLACH·Product code MAX·October 1, 2014