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Dakar

by Wenzhou Deco International Co., Ltd 7 variants

Part of a family of 17 devices: see the family page

Ref DA 11054

Dakar (DA 11054) is a Class I device made by Wenzhou Deco International Co., Ltd, registered in EUDAMED on 26 Mar 2025 (Basic UDI-DI 6974524211CV), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6974524211CV Basic UDI-DI 06974524210273UDI-DIDate26 Mar 2025RegisteredStatusActive

Official records

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  • Withdrawn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
Full rim plastic optical frames
Model / reference
DA 11054
Primary DI / UDI-DI
06974524210273
Basic UDI-DI
6974524211CV
Direct marketing DI
06974524210273
EMDN code
Q02100202 Plastic spectacle frames without lenses
Device class
Class I
EU registration type
Standard device
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
CN-MF-000005869
Authorised representative
Luxus Lebenswelt GmbH DE-AR-000005110

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Properties

Other properties (14, all answered No)