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Wózek specjalny inwalidzki AURA PRO

by Akces-Med Spółka Z Ograniczoną Odpowiedzialnością

Ref AURPRO

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59038165AURPROTW Basic UDI-DI Date24 Jun 2025RegisteredStatusActive

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  • Withdrawn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

Model / Reference
AURPRO
Primary DI / UDI-DI
05903816545510, 05903816545503, 05903816545459, 05903816545558, 05903816551313, 05903816545480, 05903816545541, 05903816551290, 05903816551306, 05903816551337, 05903816551351, 05903816539274, 05903816545534, 05903816545527, 05903816551344, 05903816539281, 05903816551276, 05903816551368, 05903816551283, 05903816551320, 05903816545466, 05903816545473
Basic UDI-DI
59038165AURPROTW
Direct Marketing DI
05903816545510
05903816545503
05903816545459
05903816545558
05903816551313
05903816545480
05903816545541
05903816551290
05903816551306
05903816551337
05903816551351
05903816539274
05903816545534
05903816545527
05903816551344
05903816539281
05903816551276
05903816551368
05903816551283
05903816551320
05903816545466
05903816545473
EMDN Code
Y122703 Pushchairs
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000003624

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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