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2004-E

by Tianjin Newtrans Technology Development

2004-E is a Class I device made by Tianjin Newtrans Technology Development, listed in FDA GUDID since 12 Jan 2023 (UDI-DI 16973881680078), registry data as of 21 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 21 Oct 2026.

Regulatory status

as of registry sync 21 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number16973881680078 UDI-DI Date12 Jan 2023ListedStatusListed 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  • Withdrawn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

Generic name
Prescription spectacles
Model / reference
2004-E
Primary DI / UDI-DI
16973881680078
FDA product code
HQY
GMDN term
Prescription spectacles
Device class
Class I
Regulation number
886.5850
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HQY (Sunglasses (Non-Prescription Including Photosensitive)).

Other devices from Tianjin Newtrans Technology Development

See all devices from Tianjin Newtrans Technology Development →

Properties

  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)