30 results
·
20ms
·
Sources: EU EUDAMED, US FDA
MINI MULTILEAF COLLIMATOR, MODEL KMI
FDA 510(k)
FDA Class 2
·Radiology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040012406·Zirlux 16+ A3 95X22
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075546·
Battalion
FDA UDI
ALPHATEC SPINE, INC.·00840967186733·Battalion, LLIF Trial, 10°, 18 mm Wide, 16 mm X...
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075614·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075645·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075553·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075591·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075577·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075584·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075638·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075607·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075560·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304075621·
DENTO-PREP PARTICLE MICROBLASTER
FDA 510(k)
FDA Class 2
·Dental
LSI SOLUTIONS FLEXIBLE SUTURE PLACEMENT DEVICE AND ACCESSORIES PRODUCT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BD BACTEC¿ MGIT¿ 960 SUPPLEMENT KIT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·August 23, 2024
SCREW LOCKING
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
RESTORE
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·April 15, 2014