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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