25 results
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35ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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VIVAPRODUCTS, INC.
FDA registration
VIVAPRODUCTS, INC.·1 product·🇺🇸 United States
Prochem
FDA UDI
VIVAPRODUCTS, INC.·00860002864815·BJP PROTEIN CONCENTRATOR 5ml - 40 TESTS
Prochem
FDA UDI
VIVAPRODUCTS, INC.·00860002864822·BJP PROTEIN CONCENTRATOR 5ml, 100 Tests
Prochem
FDA UDI
VIVAPRODUCTS, INC.·00860002864808·BJP PROTEIN CONCENTRATOR 5ml, 30 TESTS
Prochem
FDA UDI
VIVAPRODUCTS, INC.·00860002864877·BJP PROTEIN CONCENTRATOR 20ml, 100 TESTS
Prochem
FDA UDI
VIVAPRODUCTS, INC.·00860002864853·BJP PROTEIN CONCENTRATOR 10ml, 100 TESTS
Prochem
FDA UDI
VIVAPRODUCTS, INC.·00860002864846·BJP PROTEIN CONCENTRATOR 10ml, 40 TESTS
Prochem
FDA UDI
VIVAPRODUCTS, INC.·00860002864860·BJP PROTEIN CONCENTRATOR 20ml, 30 TESTS
Prochem
FDA UDI
VIVAPRODUCTS, INC.·00860002864839·BJP PROTEIN CONCENTRATOR 10ml, 30 TESTS
PRLNE BLU 24IN 8-0 D/A BV130-5 EP
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAW·September 15, 2024
PRLNE BLU 24IN 8-0 D/A BV130-5 EP
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAW·September 15, 2024
SILK BRD BLK 15X60CM M2.5
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAP·November 5, 2025
The CF-70 instrument (product code: LXG; Regulation Number: 862.2050) receives magazines containing stained blood smears from SP-50, selects only smears that require analysis, and transports them to the DI-60 for further analysis. After completing the analysis on DI-60 the smears are placed back in magazines.
FDA Recall
Terminated
·Sysmex America, Inc.·Product code LXG·March 9, 2020
EB EXC GRN 30IN 2-0 S/A V-7
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAT·August 25, 2025
PRLNE BLU 24IN 8-0 D/A BV130-5 EP
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAW·September 15, 2024
VCL CT BRD VIO 27IN 2-0 S/A SH
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAM·February 22, 2024
VCL CT BRD VIO 27IN 2-0 S/A SH
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAM·February 22, 2024
MCRYL VIO 36IN 2-0 S/A FS-1
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAN·April 2, 2025
MCRYL+ VIO 36IN 3-0 S/A FS-2
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code GAM·April 2, 2025
LEAD MODEL 304
FDA Adverse Event
Malfunction
·LIVANOVA USA, INC.·Product code LYJ·November 7, 2025