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Fielmann MC 467 CL_80269

by Fielmann Group AG

Fielmann MC 467 CL_80269 is a Class I device made by Fielmann Group AG, listed in FDA GUDID since 11 Feb 2026 (UDI-DI 04066209023437), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04066209023437 UDI-DI Date11 Feb 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Fielmann
Generic name
Spectacle frame
Model / reference
MC 467 CL_80269
Primary DI / UDI-DI
04066209023437
FDA product code
HQZ
GMDN term
Spectacle frame
Device class
Class I
Regulation number
886.5842
GUDID distribution status
In Commercial Distribution

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Properties

  • Premarket exempt
Other properties (14, all answered No)