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AI Bi

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref A01-02-122AB1Model Cassette

by Artron Laboratories Inc.

Identity

Trade Name
AI Bi EUDAMED
Device Name
Human Chorionic Gonadotropin (HCG) Test Kits for self-testing (Ultra-sensitive) EUDAMED
Model / Reference
Cassette EUDAMED
A01-02-122AB1 EUDAMED

Identifiers

Primary DI / UDI-DI
00628347568276 EUDAMED
Basic UDI-DI
B-00628347568276 EUDAMED
EMDN Code
W0102160302 HCG - RT & POC EUDAMED

Classification

Device Class
Class IVD devices for self-testing EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

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

AI Bi by Artron Laboratories Inc. — Class IVD devices for self-testing — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CA-MF-000028974
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 50176f99-f2e4-44ff-bf30-b19e55af792b 61 fields · synced Jul 9, 2026