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Newfoundland HIV Self Test

EUDAMED

Class IVD Annex II List A (EU MDR)

Ref NFLD001-02Ref NFLD001-01

by Atomo Diagnostics Limited

Identity

Trade Name
Newfoundland HIV Self Test EUDAMED
Device Name
Newfoundland HIV Self Test EUDAMED
Newfoundland HIV Self Test (ENG) EUDAMED
Model / Reference
NFLD001-02 EUDAMED
NFLD001-01 EUDAMED

Identifiers

Primary DI / UDI-DI
09349609000969 EUDAMED
09349609000938 EUDAMED
Basic UDI-DI
B-09349609000969 EUDAMED
B-09349609000938 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

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Manufacturer

EUDAMED SRN
AU-MF-000024146
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (2)

  • EUDAMED 3cc652e0-af11-4670-bb31-3fe3700aeda8 61 fields · synced Jul 27, 2026
  • EUDAMED 0a564695-15cd-46cf-b88c-9d8680cd87ed 61 fields · synced May 18, 2026