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Rexall 017276237191

by Dolgencorp, LLC

Rexall 017276237191 is a Class I device made by Dolgencorp, LLC, listed in FDA GUDID since 27 Sep 2020 (UDI-DI 00017276237191), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number00017276237191 UDI-DI Date27 Sep 2020ListedStatusListed GUDID: not 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  • Withdrawn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
Rexall
Generic name
Skin-cover adhesive strip, non-antimicrobial
Model / reference
017276237191
Primary DI / UDI-DI
00017276237191
FDA product code
KGX
GMDN term
Skin-cover adhesive strip, non-antimicrobial
Device class
Class I
Regulation number
880.5240
GUDID distribution status
Not in Commercial Distribution

Similar devices

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

Other devices from Dolgencorp, LLC

See all devices from Dolgencorp, LLC →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)