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CareOne 041520880215

by Ahold U.S.A., Inc.

CareOne 041520880215 is a non-woven gauze pad (FDA Class I; FDA product code NAB, Gauze / Sponge,Nonresorbable For External Use) made by Ahold U.S.A., Inc., listed in FDA GUDID since 28 Aug 2020 (UDI-DI 00041520880215), 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 Number00041520880215 UDI-DI Date28 Aug 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  • Withdrawn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
CareOne
Generic name
Non-woven gauze pad
Model / reference
041520880215
Primary DI / UDI-DI
00041520880215
FDA product code
NAB
GMDN term
Non-woven gauze pad
Device class
Class I
Regulation number
878.4014
GUDID distribution status
In Commercial Distribution

Related devices

Category: Non-woven gauze pad

Similar devices

Other devices filed under FDA product code NAB (Gauze / Sponge,Nonresorbable For External Use).

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)