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Lexo

EUDAMED

Class IIa (EU MDR)

Ref 15213Model G1

by Tyromotion GmbH

Identity

Trade Name
Lexo EUDAMED
Device Name
Lexo EUDAMED
Model / Reference
G1 EUDAMED
15213 EUDAMED

Identifiers

Primary DI / UDI-DI
09120077180250 EUDAMED
Basic UDI-DI
912007718LEXOBB EUDAMED
Direct Marketing DI
09120077180250 EUDAMED
EMDN Code
Z12069002 ASSISTED LOCOMOTION SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Lexo by tyromotion 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
Tyromotion GmbH
EUDAMED SRN
AT-MF-000016168

Sources (1)

  • EUDAMED 14b09bd2-3d6c-400c-8eab-d71d28ea0164 61 fields · synced Jul 9, 2026