29 results
·
37ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
RENAX HEMODIALYSIS BLOOD TUBING SET; SUNDER HEMODIALYSIS BLOOD TUBING SET
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Bard® Nelaton Catheters
FDA UDI
C. R. Bard, Inc.·10801741122542·Bard® Nelaton Catheters
CORTICAL LOCKING SCREW 3.5mm x 14mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665007817·
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0140400·Driver Shaft, T30 Final Cap Driver
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0144100·Trial, TLIF, 32L OB STR 7Deg, 10mm
SIGHT STATION
FDA UDI
FGX INTERNATIONAL INC.·00193033566138·
SIGHT STATION
FDA UDI
FGX INTERNATIONAL INC.·00193033566183·
SIGHT STATION
FDA UDI
FGX INTERNATIONAL INC.·00193033566121·
SIGHT STATION
FDA UDI
FGX INTERNATIONAL INC.·00193033566190·
SIGHT STATION
FDA UDI
FGX INTERNATIONAL INC.·00193033566145·
SIGHT STATION
FDA UDI
FGX INTERNATIONAL INC.·00193033566176·
SIGHT STATION
FDA UDI
FGX INTERNATIONAL INC.·00193033566152·
SIGHT STATION
FDA UDI
FGX INTERNATIONAL INC.·00193033566169·
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361013389·Quad Thread Cannulated 5.5x40
HRH-127 HEAD ARRAY COIL
FDA 510(k)
FDA Class 2
·Radiology
QUANTA PLEX ENA PROFILE 4
FDA 510(k)
FDA Class 2
·Immunology
COREVALVE TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·May 15, 2019
COREVALVE TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·May 22, 2020
ALLIGATOR GRASPER
FDA Adverse Event
Malfunction
·MINI-LAP TECHNOLOGIES·Product code KOG·June 30, 2014
OT PING METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013