Skip to content

Caribe Frame

by Orthos XXI, Unipessoal Lda EUDAMED 6 variants

Active European Union

Ref 80CDPOCRFR5060GGModel Caribe

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number56004569CARIBED9 Basic UDI-DIDate26 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Device Name
Cadeira de Rodas de Posicionamento
Model / Reference
Caribe, 80CDPOCRFR5060GG
Primary DI / UDI-DI
05600456991645
Basic UDI-DI
56004569CARIBED9
Direct Marketing DI
05600456991645
EMDN Code
Y122103 Push wheelchairs
Device Class
Class I
Market of Registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000002787

Other devices from Orthos XXI, Unipessoal Lda

See all devices from Orthos XXI, Unipessoal Lda →

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