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Acetate Frame

by Shenzhen Dion Eyewear Co., Ltd 75 variants

Part of a family of 70 devices: see the family page

Ref AV8085-C3

Acetate Frame (AV8085-C3) is a Class I device made by Shenzhen Dion Eyewear Co., Ltd, registered in EUDAMED on 21 Oct 2026 (Basic UDI-DI 698047810AE8), 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 Number698047810AE8 Basic UDI-DI 06980478100836UDI-DIDate21 Oct 2026RegisteredStatusActive

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  • Withdrawn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
Optical Frames
Model / reference
AV8085-C3
Primary DI / UDI-DI
06980478100836
Basic UDI-DI
698047810AE8
EMDN code
Q02100203 Metal and plastic spectacle frames without lenses
Device class
Class I
EU registration type
Standard device
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
CN-MF-000058052
Authorised representative
TESOURO D ARRASAR UNIP LDA PT-AR-000051161

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Properties

Other properties (14, all answered No)