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E2 Rapid Quantitative Test

EUDAMED

Class IVD General (EU MDR)

Ref BT2212

by Xiamen Biotime Biotechnology Co., Ltd.

Identity

Trade Name
E2 Rapid Quantitative Test EUDAMED
Device Name
E2 Rapid Quantitative Test (Fluorescence Immunoassay) EUDAMED
Model / Reference
BT2212 EUDAMED

Identifiers

Primary DI / UDI-DI
06933260208630 EUDAMED
Basic UDI-DI
B-06933260208630 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

E2 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 (2)

  • EUDAMED bff517b9-2361-4cc2-ba49-b4449770b7f5 61 fields · synced Oct 6, 2026
  • EUDAMED f4e89eec-d829-4953-90a6-5703180d9b3d 61 fields · synced Jul 14, 2026