8 results
·
27ms
·
Sources: EU EUDAMED, US FDA
LARYNGESCOPE
FDA 510(k)
FDA Class 1
·Anesthesiology
DIRECTVIEW CR Cassette with PQ Screen
FDA UDI
CARESTREAM HEALTH, INC.·60889971831989·SGL 18X24CM DIRECTVIEW PQ SCR
CEZANNE II INTERBODY FUSION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
2.4 SMARTNAIL, MODELS 532416, 532425, 532435, 532445
FDA 510(k)
FDA Class 2
·Orthopedic
SMARTNAIL
FDA Adverse Event
Injury
·CONMED CORPORATION·Product code MAI·July 29, 2019
HMO71000#QUADROX-I
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTN·March 7, 2014
32MM M2A HI CARBON HD -3MM NK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWY·November 14, 2012
840 VENTILATOR
FDA Adverse Event
Malfunction
·PURITAN BENNETT CORP.·Product code CBK·September 7, 2010