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Artlife

by Wenzhou Deco International Co., Ltd 10 variants

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

Ref 0143

Artlife (0143) 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 24 Oct 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6974524211CV Basic UDI-DI 06974524210143UDI-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  • Withdrawn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
0143
Primary DI / UDI-DI
06974524210143
Basic UDI-DI
6974524211CV
Direct marketing DI
06974524210143
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)