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COVID-19 & Influenza A+B & RSV & ADV & HMPV Antigen Combo Test Kit (LFA)

EUDAMED

Class C (EU MDR)

Ref CFRAH1NST-2Model Cassette

by Anhui Deepblue Medical Technology Co., Ltd

Identity

Trade Name
COVID-19 & Influenza A+B & RSV & ADV & HMPV Antigen Combo Test Kit (LFA) EUDAMED
Device Name
COVID-19 & Influenza A+B & RSV & ADV & HMPV Antigen Combo Test Kit (LFA) EUDAMED
Model / Reference
Cassette EUDAMED
CFRAH1NST-2 EUDAMED

Identifiers

Primary DI / UDI-DI
06952062712374 EUDAMED
Basic UDI-DI
69520627J161LM EUDAMED
Unit of Use DI
06952062713456 EUDAMED
EMDN Code
W0105070399 MULTIPLE VIRUSES - MULTIPLEX ASSAYS - OTHER EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

Yes

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

COVID-19 & Influenza A+B & RSV & ADV & HMPV Antigen Combo Test Kit (LFA) by Anhui Deepblue Medical Technology Co., Ltd — Class C — IVDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000018785
Authorised Representative
Mega Eurostar Sp. z o.o. PL-AR-000042730

Sources (1)

  • EUDAMED 95f80da6-7d23-4023-93d9-c816348df292 61 fields · synced Oct 10, 2026