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Testosterone Test (v4)

EUDAMED

Class IIa (EU MDR)

Ref TEST-01Model BT-SGRef TEST-02

by LykonDX GmbH

Identity

Trade Name
Testosterone Test (v4) EUDAMED
Model / Reference
BT-SG EUDAMED
TEST-01 EUDAMED
TEST-02 EUDAMED

Identifiers

Primary DI / UDI-DI
04260640119012 EUDAMED
04260640119005 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 (v4) 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 (2)

  • EUDAMED 1ca09bb1-aeed-43e1-bd55-abb363de605e 61 fields · synced Jul 14, 2026
  • EUDAMED e8cb5518-8847-4329-82ab-ee3378b9e71f 61 fields · synced May 18, 2026