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Giardia lamblia Rapid Test

EUDAMED

Class B (EU MDR)

Ref Format (cassette): A4B910Model Format (cassette): A4B91011 A4B910125 A4B910140 A4B91021 A4B910225 A4B910240

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

Identity

Trade Name
Giardia lamblia Rapid Test EUDAMED
Device Name
Giardia lamblia Rapid Test EUDAMED
Model / Reference
Format (cassette): A4B91011 A4B910125 A4B910140 A4B91021 A4B910225 A4B910240 EUDAMED
Format (cassette): A4B910 EUDAMED

Identifiers

Primary DI / UDI-DI
06952804832513 EUDAMED
Basic UDI-DI
69528048A4B91006X EUDAMED
EMDN Code
W0105090499 PARASITES - RT & POC - OTHER EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Spain 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

New Device

No

EUDAMED

Giardia lamblia Rapid Test by Assure Tech. (hangzhou) Co., Ltd. — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000002170
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED ca222983-e934-4f21-9e19-b94cf648ada4 61 fields · synced Jul 9, 2026