16 results
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48ms
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Sources: EU EUDAMED, US FDA
PHOENIX MEDICAL SOLUTIONS
FDA registration
PHOENIX MEDICAL SOLUTIONS·1 product·🇺🇸 United States
BD PHOENIX¿ AST INDICATOR SOLUTION
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·May 9, 2022
BD PHOENIX¿ AST-S INDICATOR SOLUTION
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·October 7, 2021
BD PHOENIX¿ AST-S INDICATOR SOLUTION
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·July 8, 2022
BD PHOENIX¿ AP AST INDICATOR SOLUTION
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·February 16, 2022
NA
FDA Adverse Event
Malfunction
·STRYKER SUSTAINABILITY SOLUTIONS PHOENIX·Product code NLH·April 20, 2020
Phoenix AST Indicator, Catalog Number 246004
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code LON·December 20, 2018
Phoenix AST-s Indicator, Catalog Number 246009
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code LON·December 20, 2018
Phoenix AP AST Indicator Bag, Catalog Number 246006
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code LON·December 20, 2018
XENIUM 150 SYNTH HF DIALYZERSYNTHETIC FOR HEMODIALYSIS
FDA Adverse Event
Injury
·NIPRO CORPORATION USD·Product code KDI·January 25, 2008
XENIUM 190 SYNTH HF DIALYZERSYNTHETIC FOR HEMODIALYSIS
FDA Adverse Event
Injury
·NIPRO CORPORATION USD·Product code KDI·January 25, 2008
Patient Guard Europe UG
Authorized representative
🇩🇪 Germany·13 Manufacturers·10 Devices
MedNet EC-REP GmbH
Authorized representative
🇩🇪 Germany·464 Manufacturers·5263 Devices
Advena Limited
Authorized representative
🇲🇹 Malta·467 Manufacturers·13717 Devices
Obelis s.a.
Authorized representative
🇧🇪 Belgium·546 Manufacturers·18515 Devices
CMC Medical Devices & Drugs SL
Authorized representative
🇪🇸 Spain·698 Manufacturers·11260 Devices