9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
THE CABOT MEDICAL INSUL-SHETH VAGINAL SPECULUM COV
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Barco
FDA UDI
Barco NV·05415334002227·MDSC-2326 DDI
ARTHROCARE PERCD SPINEWAND
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ARS SCREW; SLANT SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 28, 2013
SYNCHRON® CX9 ALX CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·December 17, 2010
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 13, 2014
EVOLUT PRO TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·October 24, 2019
EVOLUT R TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·October 24, 2019