Luxor

by Luxor Sağlik Ürünleri̇ San. Ve Ti̇c. A.Ş. 275 variants

Ref 606L

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-8698758948334QA Basic UDI-DI D-8698758948334QAUDI-DI	Date8 Apr 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device name: Silikon Topukluk L
Model / reference: 606L

Primary DI / UDI-DI: D-8698758948334QA
Basic UDI-DI: B-8698758948334QA
EMDN code: Y061203 Orthoses, foot (including insoles and inserts)

Device class: Class I
EU registration type: Legacy device (under a directive)
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: TR-MF-000021172

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Properties

Other properties (12)

Supplied sterile: No
Sterilise before use: No
Implantable: No
Reusable: No
Contains latex: No
Reprocessed single-use device: No
Incorporates a substance derived from human blood or plasma: No
Contains human tissues or cells: No
Contains animal tissues or cells: No
Administering medicine: No
Measuring function: No
Incorporates a medicinal substance: No