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Pas Pachwinowo-Przepuklinowy Obustronny “axilmax Duo”

EUDAMED

Class I (EU MDR)

Ref O-1409/LModel O-1409

by REHA FUND Sp. z o.o.

Identity

Trade Name
PAS PACHWINOWO-PRZEPUKLINOWY OBUSTRONNY “AXILMAX DUO” EUDAMED
Device Name
Pas pachwinowo-przepuklinowy obustronny „AXILMAX DUO” EUDAMED
Model / Reference
O-1409 EUDAMED
O-1409/L EUDAMED

Identifiers

Primary DI / UDI-DI
05903940709758 EUDAMED
Basic UDI-DI
59039407O1409E2 EUDAMED
Direct Marketing DI
05903940709758 EUDAMED
EMDN Code
Y060406 ABDOMINAL HERNIA SUPPORTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Pas Pachwinowo-Przepuklinowy Obustronny “axilmax Duo” by REHA FUND Sp. z o.o. — 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
PL-MF-000047481

Sources (1)

  • EUDAMED e75a5a8a-221c-4f05-ab7d-3d77543cf124 61 fields · synced Jun 18, 2026