← Back to catalogue
Aria® Dengue Ag Rapid Test
EUDAMEDClass C (EU MDR)
Ref R0063C-20T-ARModel R0063C
Identity
- Trade Name
- Aria® Dengue Ag Rapid Test EUDAMED
- Device Name
- Dengue Ag Rapid Test EUDAMED
- Model / Reference
- R0063C EUDAMEDR0063C-20T-AR EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00810114461150 EUDAMED
- Basic UDI-DI
- 081011446R0063CDU EUDAMED
- EMDN Code
- W0105040611 DENGUE VIRUS EUDAMED
Classification
- Device Class
- Class C EUDAMED
- Market of Registration
- Denmark EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
Aria® Dengue Ag Rapid Test by Ctk Biotech, Inc. — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 081011446R0063CDU | Class C | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- CTK Biotech Inc.
- EUDAMED SRN
- US-MF-000024900
- Authorised Representative
- MDSS GmbH DE-AR-000005430
Sources (1)
- EUDAMED 7eeffecf-4ed4-4026-9a75-bc8d2c3c8500 61 fields · synced Jul 17, 2026