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SP-10 Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref SP10-K02a

by Hangzhou Aichek Medical Technology Co., Ltd.

Identity

Trade Name
SP-10 Rapid Test EUDAMED
Device Name
SP-10 Rapid Test EUDAMED
Model / Reference
SP10-K02a EUDAMED

Identifiers

Primary DI / UDI-DI
D-SP10-K02aVR EUDAMED
Basic UDI-DI
B-SP10-K02aVR EUDAMED
EMDN Code
W0102160399 FERTILITY/PREGNANCY RT & POC - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

SP-10 Rapid Test by Hangzhou Aichek Medical Technology 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-000028093
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (1)

  • EUDAMED 41a522c4-3f6b-4e06-8192-259f676c7e2b 61 fields · synced Jul 13, 2026