90 results
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48ms
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Sources: EU EUDAMED, US FDA
Diagnostic Grifols, S.A.
Manufacturer
🇪🇸 Spain
Medion Grifols Diagnostics AG
Manufacturer
🇨🇭 Switzerland·5 Basic UDI-DIs·5 Devices·1 Importer
Grifols Diagnostic Solutions Inc.
Manufacturer
🇺🇸 United States
DIAGNOSTIC GRIFOLS, S.A.
FDA registration
DIAGNOSTIC GRIFOLS, S.A.·4 products·🇪🇸 Spain
ENHANCEMENT MEDIA (E.G. BOVINE ALBUMIN, LISS, PEG)
Device
EU IVDR
·
Eu Ivd Class A
·Medion Grifols Diagnostics AG·On the market·32 countries
ENHANCEMENT MEDIA (E.G. BOVINE ALBUMIN, LISS, PEG)
Device
EU IVDR
·
Eu Ivd Class A
·Medion Grifols Diagnostics AG·On the market·32 countries
IMMUNOHAEMATOLOGY (BLOOD GROUPING) TESTS - OTHER
Device
EU IVDR
·
Eu Ivd Class B
·Medion Grifols Diagnostics AG·On the market·32 countries
ENHANCEMENT MEDIA (E.G. BOVINE ALBUMIN, LISS, PEG)
Device
EU IVDR
·
Eu Ivd Class A
·Medion Grifols Diagnostics AG·On the market·32 countries
ENZYMES (E.G. BROMELIN / PAPAIN, ETC.)
Device
EU IVDR
·
Eu Ivd Class A
·Medion Grifols Diagnostics AG·On the market·32 countries
ERYTRA EFLEXIS
FDA Adverse Event
Malfunction
·DIAGNOSTIC GRIFOLS S.A.·Product code KSZ·August 5, 2024
ERYTRA EFLEXIS
FDA Adverse Event
Malfunction
·DIAGNOSTIC GRIFOLS S.A.·Product code KSZ·September 27, 2024
ERYTRA EFLEXIS
FDA Adverse Event
Malfunction
·DIAGNOSTIC GRIFOLS S.A.·Product code KSZ·September 19, 2024
ERYTRA EFLEXIS
FDA Adverse Event
Malfunction
·DIAGNOSTIC GRIFOLS, S.A.·Product code KSZ·October 31, 2025
ERYTRA EFLEXIS
FDA Adverse Event
Malfunction
·DIAGNOSTIC GRIFOLS S.A.·Product code KSZ·November 27, 2025
ERYTRA
FDA Adverse Event
Malfunction
·DIAGNOSTIC GRIFOLS S.A.·Product code KSZ·December 23, 2025
ERYTRA
FDA Adverse Event
Malfunction
·DIAGNOSTIC GRIFOLS S.A.·Product code KSZ·June 6, 2024
ERYTRA
FDA Adverse Event
Malfunction
·DIAGNOSTIC GRIFOLS, S.A.·Product code KSZ·August 8, 2023
ERYTRA
FDA Adverse Event
Malfunction
·DIAGNOSTIC GRIFOLS S.A.·Product code KSZ·September 10, 2025
DG GEL 8 A/B/D (50 CARDS)
FDA Adverse Event
Malfunction
·DIAGNOSTIC GRIFOLS S.A.·Product code QHR·September 29, 2025
ERYTRA
FDA Adverse Event
Malfunction
·DIAGNOSTIC GRIFOLS, S.A·Product code KSZ·June 4, 2020