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PRL Rapid Quantitative Test

EUDAMED

Class IVD General (EU MDR)

Ref BT2207

by Xiamen Biotime Biotechnology Co., Ltd.

Identity

Trade Name
PRL Rapid Quantitative Test EUDAMED
Device Name
PRL Rapid Quantitative Test (Fluorescence Immunoassay) EUDAMED
Model / Reference
BT2207 EUDAMED

Identifiers

Primary DI / UDI-DI
06933260208456 EUDAMED
Basic UDI-DI
B-06933260208456 EUDAMED
EMDN Code
W0102160399 FERTILITY/PREGNANCY RT & POC - OTHER 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

PRL Rapid Quantitative 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 bca67732-6760-4dd3-b012-a7bc8d9a8724 61 fields · synced Jun 18, 2026