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Tidi 9211-100

by TIDI Products, LLC.

Tidi 9211-100 is a Class I device made by TIDI Products, LLC., listed in FDA GUDID since 21 Oct 2022 (UDI-DI 00618125131327), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00618125131327 UDI-DI Date21 Oct 2022ListedStatusListed 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  • Withdrawn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
Tidi
Generic name
Eye splash shield, single-use
Model / Ref / Catalog
9211-100
Primary DI / UDI-DI
00618125131327
FDA product code
LYU
GMDN term
Eye splash shield, single-use
Device class
Class I
Regulation number
878.4040
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LYU (Accessory, Surgical Apparel).

Other devices from TIDI Products, LLC.

See all devices from TIDI Products, LLC. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
Other properties (12, all answered No)