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Testosterone Test (v3)

EUDAMED

Class IIa (EU MDR)

Ref TEST-02Model BT-SG

by LykonDX GmbH

Identity

Trade Name
Testosterone Test (v3) EUDAMED
Model / Reference
BT-SG EUDAMED
TEST-02 EUDAMED

Identifiers

Primary DI / UDI-DI
04260640119401 EUDAMED
Basic UDI-DI
4260640110000042T EUDAMED
EMDN Code
W0501010201 CAPILLARY BLOOD COLLECTION SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Medical Purpose
Entnahme und primäre Aufbewahrung einer Kapillarblutprobe durch Laienanwender in der häuslichen Umgebung. EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Testosterone Test (v3) by LykonDX GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
LykonDX GmbH
EUDAMED SRN
DE-PR-000005929

Sources (1)

  • EUDAMED e7b8f07b-3ce8-4b9d-a891-de3acb517bc0 61 fields · synced Jul 27, 2026