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SARS-CoV-2/Influenza A/Influenza B/RSV Nucleic Acid Assay Control

EUDAMED

Class IVD General (EU MDR)

Ref CRM1010302-1

by Guangzhou Pluslife Biotech Co., Ltd

Identity

Device Name
SARS-CoV-2/Influenza A/Influenza B/RSV Nucleic Acid Assay Control EUDAMED
Model / Reference
CRM1010302-1 EUDAMED

Identifiers

Primary DI / UDI-DI
06975327120271 EUDAMED
Basic UDI-DI
B-06975327120271 EUDAMED
EMDN Code
W0105094001 CONTROLS INFECTIOUS IMMUNOLOGY - RT & POC 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

SARS-CoV-2/Influenza A/Influenza B/RSV Nucleic Acid Assay Control by Guangzhou Pluslife 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-000025784
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED dcc0fd92-7bd9-4b28-a867-61a9c776bf64 61 fields · synced Oct 7, 2026