6 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SYNTHES CERVIFIX SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MyDay
FDA 510(k)
FDA Class 2
·Ophthalmic
REAGENT STRIPS FOR URINALYSIS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
ENDOTRACH TUBE 8229306J NIM EMG 6MM
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC·Product code ETN·March 6, 2013
MAXIMO II DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·February 15, 2011
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MPRI·Product code LWS·August 8, 2014