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"Serum Amyloid A Protein (SAA) Assay Test Kit (Latex immune turbidity Method)"

EUDAMED

Class IVD General (EU MDR)

Ref R1:48mL×2 R2:16mL×2(793)

by Biobase Biodustry(Shandong) Co., Ltd.

Identity

Trade Name
"Serum Amyloid A Protein (SAA) Assay Test Kit (Latex immune turbidity Method)" EUDAMED
Device Name
Serum Amyloid A Protein (SAA) Assay Test Kit (Latex immune turbidity Method) EUDAMED
Model / Reference
R1:48mL×2 R2:16mL×2(793) EUDAMED

Identifiers

Primary DI / UDI-DI
06936895300700 EUDAMED
Basic UDI-DI
B-06936895300700 EUDAMED
EMDN Code
W01010299 SUBSTRATES - OTHER 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

"Serum Amyloid A Protein (SAA) Assay Test Kit (Latex immune turbidity Method)" by Biobase Biodustry(Shandong) Co., Ltd. — Class IVD General — IVDD — listed in…

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 513a8459-b7fd-4bcf-8593-a54672bafc95 61 fields · synced Jun 19, 2026