← Back to catalogue

Combined Detection Kit for Serum Amyloid A/C-reactive Protein (SAA/CRP) (Rare e…

EUDAMED

Class IVD General (EU MDR)

Ref IF008

by Beijing Applied Biological Technologies Co., Ltd.

Identity

Device Name
Combined Detection Kit for Serum Amyloid A/C-reactive Protein (SAA/CRP) (Rare earth nano fluorescence immunochromatography) EUDAMED
Model / Reference
IF008 EUDAMED

Identifiers

Primary DI / UDI-DI
06974323014140 EUDAMED
Basic UDI-DI
B-06974323014140 EUDAMED
EMDN Code
W01021199 RHEUMATOID / INFLAMMATORY DISEASE MARKERS - 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

Combined Detection Kit for Serum Amyloid A/C-reactive Protein (SAA/CRP) (Rare e… by Beijing Applied Biological Technologies Co., Ltd. — Class IVD General…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000012338
Authorised Representative
Luxus Lebenswelt GmbH DE-AR-000005110

Sources (1)

  • EUDAMED 3e6ed764-f252-4f38-bf58-c80cbeae5d51 61 fields · synced Jul 24, 2026