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Pas Pachwinowo-Przepuklinowy Jednostronny ‘axilmax’ Czarny

by REHA FUND Sp. z o.o. 7 variants

Ref O-1408/CZA/XL/PModel O-1408

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59039407O1408DY Basic UDI-DI 05903940709642UDI-DIDate22 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Pas pachwinowo-przepuklinowy jednostronny ”AXILMAX”
Model / Reference
O-1408, O-1408/CZA/XL/P
Primary DI / UDI-DI
05903940709642
Basic UDI-DI
59039407O1408DY
Direct Marketing DI
05903940709642
EMDN Code
Y060406 Abdominal hernia supports
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000047481

Related devices

Category: Abdominal hernia truss, reusable

Other devices from REHA FUND Sp. z o.o.

See all devices from REHA FUND Sp. z o.o. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No