137 results
·
55ms
·
Sources: EU EUDAMED, US FDA
Progenika Biopharma, S.A.
Manufacturer
🇪🇸 Spain·1 Basic UDI-DI·1 Device
PROGENIKA BIOPHARMA S.A.
FDA registration
PROGENIKA BIOPHARMA S.A.·5 products·🇪🇸 Spain
Promonitor-ADL
Device
EU IVDR
·
Eu Ivd Class B
·Progenika Biopharma, S.A.·On the market·15 countries
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·March 9, 2021
Promonitor-ADL
Basic UDI-DI
EU IVDR
·
Eu Ivd Class B
·Progenika Biopharma, S.A.·1 device
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·June 30, 2021
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·April 25, 2021
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·November 26, 2021
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·July 31, 2024
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A.·Product code PEP·September 30, 2024
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·July 31, 2024
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·January 26, 2023
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·October 1, 2025
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·December 12, 2025
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·December 17, 2025
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·December 22, 2025
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·December 12, 2025
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·July 6, 2023
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA, S.A·Product code PEP·December 17, 2025
ID CORE XT
FDA Adverse Event
Malfunction
·PROGENIKA BIOPHARMA S.A.·Product code PEP·July 29, 2020