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Accufast

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref A01-06-422AF1Model Cassette

by Artron Laboratories Inc.

Identity

Trade Name
Accufast EUDAMED
Device Name
Male Fertility Sperm Tests for Self-testing EUDAMED
Model / Reference
Cassette EUDAMED
A01-06-422AF1 EUDAMED

Identifiers

Primary DI / UDI-DI
00628347568115 EUDAMED
Basic UDI-DI
B-00628347568115 EUDAMED
EMDN Code
W0102160399 FERTILITY/PREGNANCY RT & POC - OTHER EUDAMED

Classification

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

Accufast 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 485cf28f-b82d-4f3b-85d1-0ad29ae44b08 61 fields · synced Jun 19, 2026