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Walgreens 335539

by Walgreen Co.

Walgreens 335539 (WRX335539V1) is a Class I device made by Walgreen Co., listed in FDA GUDID since 14 Jul 2020 (UDI-DI 00311917164182), 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 Number00311917164182 UDI-DI Date14 Jul 2020ListedStatusListed 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  • Withdrawn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
Walgreens
Generic name
Eye patch, single-use
Model / Ref / Catalog
335539, WRX335539V1
Primary DI / UDI-DI
00311917164182
FDA product code
KGX
GMDN term
Eye patch, single-use
Device class
Class I
Regulation number
880.5240
GUDID distribution status
In Commercial Distribution
Size
Length — 2.25 Inch
Width — 3.13 Inch

Related devices

Category: Eye patch

Similar devices in this category

Other devices filed under Eye patch.

Other devices from Walgreen Co.

See all devices from Walgreen Co. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)