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Περικνημίδα Ελαστική XLarge

EUDAMED

Class I (EU MDR)

Ref 05300

by Adco Orthopaedics Ltd

Identity

Trade Name
Περικνημίδα Ελαστική XLarge EUDAMED
Device Name
Περικνημίδα Ελαστική EUDAMED
Model / Reference
05300 EUDAMED

Identifiers

Primary DI / UDI-DI
05205414131042 EUDAMED
Basic UDI-DI
5205414053003R EUDAMED
Direct Marketing DI
05205414131042 EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Greece EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

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

Περικνημίδα Ελαστική XLarge by Adco Orthopaedics Ltd — 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
GR-MF-000013663

Sources (1)

  • EUDAMED 6549976e-e5f8-4e8b-9421-215b2d15159f 61 fields · synced Oct 1, 2026