Human Parainfluenza Virus and Adenovirus Nucleic Acid Detection Kit (Real-time Fluorescence PCR Method)

by Guangzhou Deaou Gene Technology Co., Ltd 2 variants

Model 8 tests/kit

Active European Union

CE IVDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/IVDD	NumberB-06976055490124 Basic UDI-DI 06976055490124UDI-DI	Date25 Jan 2025Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/IVDD Active

Specification

EUDAMED

Device Name: Human Parainfluenza Virus and Adenovirus Nucleic Acid Detection Kit (Real-time Fluorescence PCR Method)
Model / Reference: 8 tests/kit

Primary DI / UDI-DI: 06976055490124
Basic UDI-DI: B-06976055490124
EMDN Code: W0105070503 Respiratory tract infections - multiplex na reagents

Device Class: Class IVD General
EU market of registration: Spain

Manufacturer details

EUDAMED SRN: CN-MF-000033028
Authorised representative: RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

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Properties

Reagent
Professional Testing

Other properties (8)

Sterile: No
Human Tissues: No
Animal Tissues: No
Microbial Substances: No
Self Testing: No
Near-Patient Testing: No
Companion Diagnostics: No
Surgical Instrument: No