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Op-2240-4

EUDAMED

Class I (EU MDR)

Ref OP-2240-4Model OP-1000 /.../ OP-2505

by Europack Uluslararasi Sağlik Ve Spor Ürünleri Anoni̇m Şi̇rketi̇

Identity

Trade Name
OP-2240-4 EUDAMED
Device Name
ORTHOPEDICS SUPPORT ORTHOSES EUDAMED
Model / Reference
OP-1000 /.../ OP-2505 EUDAMED
OP-2240-4 EUDAMED

Identifiers

Primary DI / UDI-DI
08683907245211 EUDAMED
Basic UDI-DI
86839072OP001SW EUDAMED
Direct Marketing DI
08683907245211 EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT ORTHOSES 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

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

Category: Ankle/foot orthosis

Op-2240-4 by Europack Uluslararasi Sağlik Ve Spor Ürünleri Anoni̇m Şi̇rketi̇ — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ankle/foot orthosis.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
TR-MF-000038879

Sources (1)

  • EUDAMED bc86a4d8-ad91-4272-8990-50f7e0034282 61 fields · synced Oct 6, 2026