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Multi- Drug Rapid Test

EUDAMED

Class B (EU MDR)

Ref DOA-N144-016

by Hangzhou Alltest Biotech.Co., Ltd.

Identity

Trade Name
Multi- Drug Rapid Test EUDAMED
Device Name
Multi- Drug Rapid Test EUDAMED
Model / Reference
DOA-N144-016 EUDAMED

Identifiers

Primary DI / UDI-DI
06936983141680 EUDAMED
Basic UDI-DI
6970277510007AXY EUDAMED
EMDN Code
W0102160511 MULTIPLE DRUGS OF ABUSE/TOXICOLOGY RT & POC EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Ireland 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

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Multi- Drug Rapid Test by Hangzhou Alltest Biotech.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-000010710
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 0f8c58d2-8207-4df9-a625-0c74058cd92f 61 fields · synced Jul 14, 2026