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Pas Pachwinowo-Przepuklinowy Jednostronny ‘axilmax’

EUDAMED

Class I (EU MDR)

Ref O-1408/S/PModel O-1408Ref O-1408/S/LRef O-1408/L/LRef O-1408/M/LRef O-1408/CZA/M/LRef O-1408/L/PRef O-1408/CZA/S/PRef O-1408/CZA/S/LRef O-1408/CZA/XL/P

by REHA FUND Sp. z o.o.

Identity

Trade Name
PAS PACHWINOWO-PRZEPUKLINOWY JEDNOSTRONNY ‘AXILMAX’ EUDAMED
PAS PACHWINOWO-PRZEPUKLINOWY JEDNOSTRONNY ‘AXILMAX’ CZARNY EUDAMED
Device Name
Pas pachwinowo-przepuklinowy jednostronny ”AXILMAX” EUDAMED
Model / Reference
O-1408 EUDAMED
O-1408/S/P EUDAMED
O-1408/S/L EUDAMED
O-1408/L/L EUDAMED
O-1408/M/L EUDAMED
O-1408/CZA/M/L EUDAMED
O-1408/L/P EUDAMED
O-1408/CZA/S/P EUDAMED
O-1408/CZA/S/L EUDAMED
O-1408/CZA/XL/P EUDAMED

Identifiers

Primary DI / UDI-DI
05903940709574 EUDAMED
05903940709659 EUDAMED
05903940709673 EUDAMED
05903940709666 EUDAMED
05903940709703 EUDAMED
05903940709598 EUDAMED
05903940709611 EUDAMED
05903940709697 EUDAMED
05903940709642 EUDAMED
Basic UDI-DI
59039407O1408DY EUDAMED
Direct Marketing DI
05903940709574 EUDAMED
05903940709659 EUDAMED
05903940709673 EUDAMED
05903940709666 EUDAMED
05903940709703 EUDAMED
05903940709598 EUDAMED
05903940709611 EUDAMED
05903940709697 EUDAMED
05903940709642 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 Jednostronny ‘axilmax’ 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 (9)

  • EUDAMED 7c64b26e-50b5-492f-a8f2-d52c24c762fa 61 fields · synced Oct 6, 2026
  • EUDAMED 5eed6696-9d60-4e35-9358-d52058048b95 61 fields · synced May 17, 2026
  • EUDAMED 6f3b2cce-3ec3-4b78-90db-c52bfcfa129e 61 fields · synced May 17, 2026
  • EUDAMED 707b70c6-b9bc-4f2a-8b9d-93314d5eb110 61 fields · synced May 18, 2026
  • EUDAMED 52a7aa69-94c8-458b-b8a2-3b3115a7e868 61 fields · synced May 18, 2026
  • EUDAMED c0b4159b-7339-423f-9a33-3ed146f40aa1 61 fields · synced May 18, 2026
  • EUDAMED c3161e41-7c1f-4461-812c-eb2552c133fb 61 fields · synced May 18, 2026
  • EUDAMED 35143d4b-952d-4b64-84fa-d21757b3d892 61 fields · synced May 19, 2026
  • EUDAMED 6c87ff66-7a5e-475d-89c5-a8dd5a3fb85b 61 fields · synced May 19, 2026