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Acmex Human Immunodeficiency Virus 1/2 (HIV1/2) Antibody Test

EUDAMED

Class D (EU MDR)

Ref AM02-07-322P25Model Cassette

by Artron Laboratories Inc.

Identity

Trade Name
Acmex Human Immunodeficiency Virus 1/2 (HIV1/2) Antibody Test EUDAMED
Device Name
Human Immunodeficiency Virus (HIV 1/2) Antibody Test EUDAMED
Model / Reference
Cassette EUDAMED
AM02-07-322P25 EUDAMED

Identifiers

Primary DI / UDI-DI
00628347561048 EUDAMED
Basic UDI-DI
62834756AL0207026X EUDAMED
EMDN Code
W0105090302 HIV 1 / 2 - RT & POC EUDAMED

Classification

Device Class
Class D EUDAMED
Market of Registration
Hungary EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Acmex Human Immunodeficiency Virus 1/2 (HIV1/2) Antibody Test by Artron Laboratories Inc. — Class D — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

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

Sources (1)

  • EUDAMED 3e1e166f-1656-4af7-8da0-2811724446ea 61 fields · synced Jun 19, 2026