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Specific Albumin 30%

EUDAMED

Class A (EU MDR)

Ref 213573Model Specific Albumin 30%

by Medion Grifols Diagnostics AG

Identity

Trade Name
Specific Albumin 30% EUDAMED
Device Name
Specific Albumin 30% EUDAMED
Model / Reference
Specific Albumin 30% EUDAMED
213573 EUDAMED

Identifiers

Primary DI / UDI-DI
07640137341107 EUDAMED
Basic UDI-DI
764013734Albumin-002CW EUDAMED
Direct Marketing DI
07640137341107 EUDAMED
EMDN Code
W0103030306 ENHANCEMENT MEDIA (E.G. BOVINE ALBUMIN, LISS, PEG) 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

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Specific Albumin 30% by Medion Grifols Diagnostics Ag — 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
CH-MF-000024272
Authorised Representative
Diagnostic Grifols, S.A. ES-AR-000001573

Sources (2)

  • EUDAMED 9d79a388-41c7-4c9b-805a-f8221388cb10 61 fields · synced Jul 14, 2026
  • EUDAMED 004dc3bb-ed0e-42ea-bf83-cf022faf701c 61 fields · synced Jul 14, 2026