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Kösemed

EUDAMED

Class I (EU MDR)

Ref 605-04

by Kösemed Ortopedi̇ San. Ve Ti̇c. İth. İhr. A.ş.

Identity

Trade Name
Kösemed EUDAMED
Device Name
Silikon Tabanlık Kumaşlı L EUDAMED
Model / Reference
605-04 EUDAMED

Identifiers

Primary DI / UDI-DI
D-868203550021654 EUDAMED
Basic UDI-DI
B-868203550021654 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

Category: Orthotic insole, prefabricated, non-antimicrobial

Kösemed by Kösemed Ortopedi̇ San. Ve Ti̇c. İth. İhr. A.ş. — Class I — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthotic insole, prefabricated, non-antimicrobial.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TR-MF-000021022

Sources (1)

  • EUDAMED 656c5bc3-8371-4707-a9f0-c7886526afaa 61 fields · synced Oct 6, 2026