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Malaria P.f/P.v Antigen Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref BT0102101

by Xiamen Biotime Biotechnology Co., Ltd.

Identity

Trade Name
Malaria P.f/P.v Antigen Rapid Test EUDAMED
Device Name
Malaria P.f/P.v Antigen Rapid Test EUDAMED
Model / Reference
BT0102101 EUDAMED

Identifiers

Primary DI / UDI-DI
06933260206339 EUDAMED
Basic UDI-DI
B-06933260206339 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/P.v 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 (2)

  • EUDAMED 38722805-e825-4411-88a0-e97ee661daa4 61 fields · synced Aug 1, 2026
  • EUDAMED c7dbfda8-1dd7-410f-ad58-e06650adbc3b 61 fields · synced Aug 1, 2026