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Rinderalbumin 22%

EUDAMED

Class A (EU MDR)

Ref 805060

by Bio-Rad Medical Diagnostics GmbH

Identity

Trade Name
Rinderalbumin 22% EUDAMED
Device Name
Rinderalbumin 22% EUDAMED
Model / Reference
805060 EUDAMED

Identifiers

Primary DI / UDI-DI
07611969950812 EUDAMED
Basic UDI-DI
361052A002938E EUDAMED
EMDN Code
W0103030306 ENHANCEMENT MEDIA (E.G. BOVINE ALBUMIN, LISS, PEG) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

Rinderalbumin 22% by Bio-Rad Medical Diagnostics Gmbh — 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
DE-MF-000019864

Sources (1)

  • EUDAMED e9c594b4-2187-4964-8130-a7decb177ce2 61 fields · synced Jul 9, 2026