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SARS-CoV-2/InFluA/InFluB Rapid Antigen Test (Immunochromatography Assay)
EUDAMEDClass IVD General (EU MDR)
Ref S3121E-25
Identity
- Device Name
- SARS-CoV-2/InFluA/InFluB Rapid Antigen Test (Immunochromatography Assay) EUDAMED
- Model / Reference
- S3121E-25 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06955792730526 EUDAMED
- Basic UDI-DI
- B-06955792730526 EUDAMED
- EMDN Code
- W0105070399 MULTIPLE VIRUSES - MULTIPLEX ASSAYS - OTHER EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Greece EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
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/InFluA/InFluB Rapid Antigen Test (Immunochromatography Assay) by Sansure Biotech Inc. — Class IVD General — IVDD — listed in EUDAMED
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-06955792730526 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- Sansure Biotech Inc.
- EUDAMED SRN
- CN-MF-000011392
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (1)
- EUDAMED 0cc31879-8325-4650-abc6-44c6cc190dad 61 fields · synced Jul 30, 2026