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COVID-19 (Sars-CoV-2) Antigen Test Midstream - Saliva

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref COVAg3SST-X

by Anhui Deepblue Medical Technology Co., Ltd

Identity

Trade Name
COVID-19 (Sars-CoV-2) Antigen Test Midstream - Saliva EUDAMED
Device Name
COVID-19 (Sars-CoV-2) Antigen Test Midstream - Saliva EUDAMED
Model / Reference
COVAg3SST-X EUDAMED

Identifiers

Primary DI / UDI-DI
06952062772781 EUDAMED
Basic UDI-DI
B-06952062772781 EUDAMED
EMDN Code
W0105099099 VIROLOGY - RT & POC - OTHER EUDAMED

Classification

Device Class
Class IVD devices for self-testing EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

Yes

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

COVID-19 (Sars-CoV-2) Antigen Test Midstream - Saliva by Anhui Deepblue Medical Technology Co., Ltd — Class IVD devices for self-testing — IVDD — listed in…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000018785
Authorised Representative
Luxus Lebenswelt GmbH DE-AR-000005110

Sources (1)

  • EUDAMED afaa9381-6351-48a8-8bf2-5a218325cb18 61 fields · synced Oct 6, 2026