30 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TINA-QUANT COMPLEMENT C4 TEST SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
G-aenial™
FDA UDI
Gc America Inc.·D0470123591·G-aenial Univ. Injectable Unitip AO3
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033397817·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033397787·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033397848·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033397824·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033397831·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033397855·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033397800·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033397794·
MDI GLIADIN G TEST
FDA 510(k)
FDA Class 2
·Immunology
INNOVO
FDA 510(k)
FDA Class 2
·General Hospital
0009613348-2024-012359
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code DZE·September 16, 2024
ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·January 9, 2019
ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·September 26, 2018
UNKNOWN VERSASTEP
FDA Adverse Event
Malfunction
·COVIDIEN·Product code GCJ·June 11, 2015
ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·December 10, 2019
ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·July 30, 2019
TAXUS¿ LIBERTÉ¿ LONG
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·March 20, 2013
KIMVENT MICROCUFF ENDOTRACHEAL TUBE
FDA Adverse Event
Malfunction
·KIMBERLY-CLARK HEALTH CARE·Product code BTR·March 9, 2011