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Daniel Hechter HEP004-2

by MPG GmbH

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 Number09009507511751 UDI-DI Date20 Sep 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Daniel Hechter
Generic name
Spectacle frame
Model / reference
HEP004-2
Primary DI / UDI-DI
09009507511751
FDA product code
HQZ
GMDN term
Spectacle frame
Device class
Class I
Regulation number
886.5842
GUDID distribution status
In Commercial Distribution

Related devices

Category: Spectacle frame

Other devices from MPG GmbH

See all devices from MPG GmbH →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date

Other properties (12)

  • 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
  • Serial number: No
  • Expiration date: No