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Luxor

EUDAMED

Class I (EU MDR)

Ref 605S

by Luxor Sağlik Ürünleri̇ San. Ve Ti̇c. A.ş.

Identity

Trade Name
Luxor EUDAMED
Device Name
Silikon Tabanlık Kumaşlı S EUDAMED
Model / Reference
605S EUDAMED

Identifiers

Primary DI / UDI-DI
D-8698758945036PA EUDAMED
Basic UDI-DI
B-8698758945036PA EUDAMED
EMDN Code
Y061203 ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Luxor by Luxor Sağlik Ürünleri̇ San. Ve Ti̇c. A.ş. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TR-MF-000021172

Sources (1)

  • EUDAMED 07214778-e749-475b-91c9-c6fe0c43c6dd 61 fields · synced Oct 7, 2026