977 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VITEK® 2 GN TEST KIT
FDA Adverse Event
Malfunction
·BIOMÉRIEUX, INC·Product code LQM·July 29, 2019
BD PHOENIX¿ NID
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LQM·June 23, 2023
BD PHOENIX¿ NID
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LQM·June 27, 2023
NEG URINE COMBO 61
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code LQM·July 28, 2015
NEG COMBO PANEL TYPE 50
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code LQM·July 9, 2015
NEG URINE COMBO 61
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code LQM·July 28, 2015
NEG URINE COMBO 61
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code LQM·July 28, 2015
VITEK® 2 GN TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code LQM·December 21, 2017
VITEK® 2 GN TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code LQM·December 5, 2017
VITEK® 2 GN ID TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX INC.·Product code LQM·November 10, 2017
VITEK®2 GN TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX INC.·Product code LQM·December 4, 2017
VITEK® 2 GN TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code LQM·December 27, 2017
VITEK® 2 GN ID TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LQM·November 27, 2017
VITEK® 2 GN ID TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LQM·November 2, 2017
VITEK® 2 GRAM NEGATIVE ID TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LQM·October 13, 2017
VITEK®2 GRAM NEGATIVE TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX INC.·Product code LQM·October 5, 2017
VITEK®2 GN TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX INC.·Product code LQM·December 4, 2017
VITEK® 2 GN ID TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LQM·November 20, 2017
VITEK® 2 GN ID TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code LQM·November 22, 2017
VITEK® 2 GN TEST KIT
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC·Product code LQM·December 21, 2017