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Celta

by Orthos XXI, Unipessoal Lda 15 variants

Ref 51CDCE2NO43NP, 51CDCE2NO40NM, 51CDCE2NO40ND, 51CDCE2NO50ED, 51CDC32AE46AM, 51CDCE2NO46NP, 51CDC32NO54EM, 51CDCECONFIG, 51CDCEESPECIAL, 51CDCE2NO37EM, 51CDCE2NO37ND, 51CDC32NO40EM, 51CDCE2NO40NP, 51CDC32NO58EM, 51CDC32AE54AM, 51CDCE2NO43ND, 51CDC32AE40AM, 51CDCE2NO46ND, 51CDC32AE43AM, 51CDC32NO37EM, 51CDC32AE58AM, 51CDCE2NO37ED, 51CDCE2NO40EM, 51CDCE4NO37ND, 51CDCE6NO37ND, 51CDCPESPECIAL, 51CDCE6NO40ND, 51CDCE6NO43NDModel Celta

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number56004569CELTAG7 Basic UDI-DI Date26 Mar 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  • Withdrawn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

Trade Name
Celta
Celta Compact 3 Transit
Celta Compact 3
Device Name
Cadeira de Rodas
Model / Reference
Celta, 51CDCE2NO43NP, 51CDCE2NO40NM, 51CDCE2NO40ND, 51CDCE2NO50ED, 51CDC32AE46AM, 51CDCE2NO46NP, 51CDC32NO54EM, 51CDCECONFIG, 51CDCEESPECIAL, 51CDCE2NO37EM, 51CDCE2NO37ND, 51CDC32NO40EM, 51CDCE2NO40NP, 51CDC32NO58EM, 51CDC32AE54AM, 51CDCE2NO43ND, 51CDC32AE40AM, 51CDCE2NO46ND, 51CDC32AE43AM, 51CDC32NO37EM, 51CDC32AE58AM, 51CDCE2NO37ED, 51CDCE2NO40EM, 51CDCE4NO37ND, 51CDCE6NO37ND, 51CDCPESPECIAL, 51CDCE6NO40ND, 51CDCE6NO43ND
Primary DI / UDI-DI
05600456901187, 05600456901118, 05600456901125, 05600456901460, 05600456900739, 05600456901231, 05600456903204, 05600456900777, 05600456900784, 05600456901095, 05600456901071, 05600456900562, 05600456901132, 05600456903211, 05600456903235, 05600456901170, 05600456900715, 05600456901224, 05600456900722, 05600456900548, 05600456903242, 05600456901101, 05600456901149, 05600456900982, 05600456901026, 05600456900418, 05600456901033, 05600456901040
Basic UDI-DI
56004569CELTAG7
Direct Marketing DI
05600456901187
05600456901118
05600456901125
05600456901460
05600456900739
05600456901231
05600456903204
05600456900777
05600456900784
05600456901095
05600456901071
05600456900562
05600456901132
05600456903211
05600456903235
05600456901170
05600456900715
05600456901224
05600456900722
05600456900548
05600456903242
05600456901101
05600456901149
05600456900982
05600456901026
05600456900418
05600456901033
05600456901040
EMDN Code
Y122106, Y122103
Device Class
Class I
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000002787

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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