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Kroger 041260020803

by Kroger Co., the

Kroger 041260020803 is a device classified as Not classified made by Kroger Co., the, listed in FDA GUDID since 15 Apr 2024 (UDI-DI 00041260020803), 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 Number00041260020803 UDI-DI Date15 Apr 2024ListedStatusListed 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  • Withdrawn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
Kroger
Generic name
First aid kit, medicated
Model / reference
041260020803
Primary DI / UDI-DI
00041260020803
FDA product code
LRR
GMDN term
First aid kit, medicated
Device class
N
GUDID distribution status
In Commercial Distribution

Related devices

Category: First aid kit, medicated

Similar devices

Other devices filed under FDA product code LRR (First Aid Kit With Drug).

Other devices from Kroger Co., the

See all devices from Kroger Co., the →

Properties

  • Over-the-counter
  • Convenience kit
  • Combination product
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)