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Κηλεπίδεσμος Διπλός XXLarge

EUDAMED

Class I (EU MDR)

Ref 04310

by Adco Orthopaedics Ltd

Identity

Trade Name
Κηλεπίδεσμος Διπλός XXLarge EUDAMED
Device Name
Κηλεπίδεσμος Διπλός EUDAMED
Model / Reference
04310 EUDAMED

Identifiers

Primary DI / UDI-DI
05205414082054 EUDAMED
Basic UDI-DI
5205414043103M EUDAMED
Direct Marketing DI
05205414082054 EUDAMED
EMDN Code
Y060406 ABDOMINAL HERNIA SUPPORTS 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: Abdominal hernia truss, reusable

Κηλεπίδεσμος Διπλός XXLarge by Adco Orthopaedics Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Abdominal hernia truss, reusable.

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 6ec97864-fd8c-4df4-8df0-32eaa07081e8 61 fields · synced Jun 19, 2026