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Erytra

EUDAMED

Class A (EU MDR)

Ref 210400

by Diagnostic Grifols, S.A.

Identity

Trade Name
Erytra EUDAMED
Device Name
Erytra EUDAMED
Model / Reference
210400 EUDAMED

Identifiers

Primary DI / UDI-DI
08436583730935 EUDAMED
Basic UDI-DI
843658373ERYTRAVJ EUDAMED
EMDN Code
W0202030102 AUTOMATED BLOOD GROUPING ANALYSERS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Erytra by Diagnostic Grifols, S.a. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
ES-MF-000000784

Sources (1)

  • EUDAMED 2bafa130-23f9-435f-a157-54ad4ac20cc0 61 fields · synced Oct 6, 2026