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Albumin (ALB) Test Kit (BCG )

EUDAMED

Class IVD General (EU MDR)

Ref R:50mL×4(791)

by Biobase Biodustry(Shandong) Co., Ltd.

Identity

Trade Name
Albumin (ALB) Test Kit (BCG ) EUDAMED
Device Name
Albumin (ALB) Test Kit (BCG ) EUDAMED
Model / Reference
R:50mL×4(791) EUDAMED

Identifiers

Primary DI / UDI-DI
06971674862499 EUDAMED
Basic UDI-DI
B-06971674862499 EUDAMED
EMDN Code
W0102010309 ALBUMIN (IC) INCL. UALBUMIN EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany 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

Albumin (ALB) Test Kit (BCG ) by Biobase Biodustry(Shandong) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000025015
Authorised Representative
Luxus Lebenswelt GmbH DE-AR-000005110

Sources (1)

  • EUDAMED 062ca557-77ae-45ba-ac6b-d1446dd430ae 61 fields · synced Jun 18, 2026