Skip to content

Fielmann MC 176 TR_79510

by Fielmann Group AG

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04066209019676 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  • Withdrawn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 176 TR_79510
Primary DI / UDI-DI
04066209019676
FDA product code
HQZ
GMDN term
Spectacle frame
Device class
Class I
Regulation number
886.5842
GUDID distribution status
In Commercial Distribution

Other devices from Fielmann Group AG

See all devices from Fielmann Group AG →

Properties

  • Premarket exempt

Other properties (14)

  • Supplied sterile: No
  • Sterilise before use: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Lot / batch number: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No