24 results
·
28ms
·
Sources: EU EUDAMED, US FDA
MODIFICATION TO ENSITE 3000 SYSTEM, MODEL EE3000
FDA 510(k)
FDA Class 2
·Cardiovascular
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304138005·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304138043·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304138074·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304138012·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304138067·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304138098·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304138104·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304138050·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304138029·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304138081·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304138036·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304138111·
R-SI-LINE METAL-BITE
FDA 510(k)
FDA Class 2
·Dental
ELEC-MATE E
FDA 510(k)
FDA Class 1
·Dental
0009613348-2024-012926
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code DZE·September 30, 2024
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·October 16, 2024
A7 ANESTHESIA SYSTEM
FDA Adverse Event
Malfunction
·SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO. LTD.·Product code BSZ·February 15, 2017
LEADER 1CC X 31G INS SYR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FMF·February 25, 2013
TAXUS LIBERTE ATOM PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·March 10, 2011