10,000 results
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37ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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BACTEC FOS CULTURE SUPPLEMENT
FDA 510(k)
FDA Class 1
·Microbiology
Curaplex
FDA UDI
BOUND TREE MEDICAL, LLC·00812277037883·HANDLE,STANDARD,DISP.,CURAVIEW FO,GREEN SYSTEM
BD BACTEC™ FOS™ Culture Supplement Kit
FDA UDI
BECTON, DICKINSON AND COMPANY·30382904421534·BD BACTEC™ FOS™ Culture Supplement Kit
AUTOCAT2 WAVE
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code DSP·August 21, 2009
AUTOCAT2 WAVE
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code DSP·February 27, 2017
AC3 OPTIMUS IABP NA/EMEA
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL LLC·Product code DSP·May 19, 2023
AUTOCAT2 WAVE ITALIAN
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code DSP·October 21, 2015
AUTOCAT2 WAVE
FDA Adverse Event
Malfunction
·ARROW INT'L., INC.·Product code DSP·November 20, 2009
BD BACTEC¿ FOS¿ CULTURE SUPPLEMENT KIT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·September 3, 2025
BD BACTEC¿ FOS¿ CULTURE SUPPLEMENT KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·September 2, 2025
BD BACTEC¿ FOS¿ (FASTIDIOUS ORGANISM SUPPLEMENT) KIT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·April 16, 2024
BD BACTEC¿ FOS¿ (FASTIDIOUS ORGANISM SUPPLEMENT) KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·July 27, 2021
BD BACTEC¿ FOS¿ CULTURE SUPPLEMENT KIT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·February 7, 2025
AUTOCAT2 WAVE
FDA Adverse Event
Malfunction
·ARROW INTL., INC.·Product code DSP·May 9, 2008
AUTOCAT 2 WAVE JAPANESE
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC·Product code DSP·December 1, 2011
AUTOCAT2 WAVE
FDA Adverse Event
Malfunction
·ARROW INTL., INC.·Product code DSP·December 8, 2009
BD BACTEC¿ FOS¿ CULTURE SUPPLEMENT KIT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·August 13, 2024
FIBEROPTIX ULTRA 8 IAB: 8FR 40CC
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code DSP·December 1, 2016
AUTOCAT2 WAVE
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code DSP·April 9, 2018
AUTOCAT2 WAVE
FDA Adverse Event
Malfunction
·ARROW INTL., INC.·Product code DSP·July 20, 2011