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Newfoundland HIV Self Test
EUDAMEDClass IVD Annex II List A (EU MDR)
Ref NFLD001-03
Identity
- Device Name
- Newfoundland HIV Self Test EUDAMED
- Model / Reference
- NFLD001-03 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 09349609001102 EUDAMED
- Basic UDI-DI
- B-09349609001102 EUDAMED
- EMDN Code
- W0105030402 HIV MULTIPLE ANTIBODY EUDAMED
Classification
- Device Class
- Class IVD Annex II List A EUDAMED
- Market of Registration
- Belgium EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
Yes
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
Newfoundland HIV Self Test by Atomo Diagnostics Limited — Class IVD Annex II List A — IVDD — listed in EUDAMED — regulatory data on deviCERTS
Manufacturer's product page: Download Factsheet
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-09349609001102 | Class IVD Annex II List A | Active |
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Manufacturer
- Manufacturer
- Atomo Diagnostics Limited
- EUDAMED SRN
- AU-MF-000024146
- Authorised Representative
- QbD RepS BV BE-AR-000000040
Sources (1)
- EUDAMED 527af14d-f82c-48c5-91ef-ddb541c9c270 61 fields · synced Jun 19, 2026