8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
MILL-ROSE ROTATABLE POLYPECTOMY SNARE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PHARMACIA DELTA CADD PUMP
FDA Adverse Event
Injury
·PHARMACIA DELTEC, INC.·Product code FRN·August 8, 1995
R-40 EEG Amplifier
FDA 510(k)
FDA Class 2
·Neurology
SYNTHES (USA) DISTRACTION OSTEOGENESIS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PULSE-GENERATOR, PACEMAKER, EXTERNAL
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA, INC.·Product code DTE·February 9, 2013
OT VERIO PRO PLUS METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014
CONTAK RENEWAL
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 6, 2011
VERSA-DIAL SHOULDER SYSTEM MODULAR HEAD 50MM X 24MM X 52MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBF·October 28, 2016