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Malaria P.f Antigen Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref BT0101901

by Xiamen Biotime Biotechnology Co., Ltd.

Identity

Trade Name
Malaria P.f Antigen Rapid Test EUDAMED
Device Name
Malaria P.f Antigen Rapid Test EUDAMED
Model / Reference
BT0101901 EUDAMED

Identifiers

Primary DI / UDI-DI
06933260206315 EUDAMED
Basic UDI-DI
B-06933260206315 EUDAMED
EMDN Code
W0105050209 PLASMODIUM (MALARIA) EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands 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

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Malaria P.f Antigen Rapid Test by Xiamen Biotime Biotechnology 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-000012852
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (1)

  • EUDAMED 6021e237-9c84-47e5-837e-d381f059574f 61 fields · synced Jun 18, 2026