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CareOne 041520863461

by Ahold U.S.A., Inc.

CareOne 041520863461 is a Class I device made by Ahold U.S.A., Inc., listed in FDA GUDID since 31 Jul 2019 (UDI-DI 00041520863461), 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 Number00041520863461 UDI-DI Date31 Jul 2019ListedStatusListed 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  • Withdrawn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
CareOne
Generic name
Skin-closure adhesive strip
Model / reference
041520863461
Primary DI / UDI-DI
00041520863461
FDA product code
KGX
GMDN term
Skin-closure adhesive strip
Device class
Class I
Regulation number
880.5240
GUDID distribution status
In Commercial Distribution

Related devices

Category: Skin-closure adhesive strip

Similar devices

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

Other devices from Ahold U.S.A., Inc.

See all devices from Ahold U.S.A., Inc. →

Properties

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