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Σλίπ Κήλης XLarge

EUDAMED

Class I (EU MDR)

Ref 04312

by Adco Orthopaedics Ltd

Identity

Trade Name
Σλίπ Κήλης XLarge EUDAMED
Device Name
Σλίπ Κήλης EUDAMED
Model / Reference
04312 EUDAMED

Identifiers

Primary DI / UDI-DI
05205414084041 EUDAMED
Basic UDI-DI
5205414043123R EUDAMED
Direct Marketing DI
05205414084041 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

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: Abdominal hernia truss, reusable

Σλίπ Κήλης XLarge 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 87b0b2b4-b5c6-41cf-9269-0f20468e56cd 61 fields · synced Jun 19, 2026