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Kroger 041260008726

by Kroger Co., the

Kroger 041260008726 is a Class I device made by Kroger Co., the, listed in FDA GUDID since 29 Apr 2020 (UDI-DI 00041260008726), 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 Number00041260008726 UDI-DI Date29 Apr 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  • Withdrawn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
Kroger
Generic name
Pressure bandage, non-latex, single-use
Model / reference
041260008726
Primary DI / UDI-DI
00041260008726
FDA product code
KGX
GMDN term
Pressure bandage, non-latex, single-use
Device class
Class I
Regulation number
880.5240
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pressure bandage, non-latex, single-use

Similar devices

Other devices filed under FDA product code KGX (Tape And Bandage, Adhesive).

Other devices from Kroger Co., the

See all devices from Kroger Co., the →

Properties

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