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Zika NS1 Antigen Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref ZIKA-NS1-W23

by Assure Tech. (Hangzhou) Co., Ltd.

Identity

Device Name
Zika NS1 Antigen Rapid Test EUDAMED
Model / Reference
ZIKA-NS1-W23 EUDAMED

Identifiers

Primary DI / UDI-DI
D-ZIKANS1-W23YD EUDAMED
Basic UDI-DI
B-ZIKANS1-W23YD EUDAMED
EMDN Code
W0105099099 VIROLOGY - 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

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Zika NS1 Antigen Rapid Test by Assure Tech. (hangzhou) 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-000002170
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 9520dd9d-14d7-49a3-ad6a-37a899d86446 61 fields · synced Jun 19, 2026