405 Xl

by Aurafi̇x Health Products Diş Ti̇caret Ve Sanayi̇ Anoni̇m Şi̇rketi̇

Ref 405 XLModel ORTHOPEDIC ANKLE BRACES

Active European Union

CE MDR

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number86803954ORT08XB Basic UDI-DI 08698779834715UDI-DI	Date10 Mar 2025Registered	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Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference: ORTHOPEDIC ANKLE BRACES, 405 XL

Primary DI / UDI-DI: 08698779834715
Basic UDI-DI: 86803954ORT08XB
Direct Marketing DI: 08698779834715
EMDN Code: Y06120601 Passive ankle-foot orthoses

Device Class: Class I
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: TR-MF-000046503

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Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No