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2-IN-1 COVID-19 Antigen Rapid Test Device (Nasal&Saliva)

EUDAMED

Class IVD General (EU MDR)

Ref A151601D

by Hangzhou Cybereagen Biotech Co., Ltd.

Identity

Trade Name
2-IN-1 COVID-19 Antigen Rapid Test Device (Nasal&Saliva) EUDAMED
Model / Reference
A151601D EUDAMED

Identifiers

Primary DI / UDI-DI
06976753472989 EUDAMED
Basic UDI-DI
B-06976753472989 EUDAMED
EMDN Code
W0105040619 EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany 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

2-IN-1 COVID-19 Antigen Rapid Test Device (Nasal&Saliva) by Hangzhou Cybereagen Biotech Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000037850
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED e36fce75-af8c-443d-bfdf-7e5b6ddc6cc7 61 fields · synced Oct 7, 2026