Care One 055076

by Ahold U.S.A., Inc.

Care One 055076 is a multiple drugs of abuse IVD (FDA Class II; FDA product code LDJ, Enzyme Immunoassay, Cannabinoids) made by Ahold U.S.A., Inc., listed in FDA GUDID since 26 Aug 2021 (UDI-DI 00041520113375), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00041520113375 UDI-DI	Date26 Aug 2021Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00041520113375

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Care One
Generic name: Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Model / reference: 055076

Primary DI / UDI-DI: 00041520113375
FDA product code: LDJ
GMDN term: Multiple drugs of abuse IVD, kit, rapid ICT, clinical

Device class: Class II
Regulation number: 862.3870
GUDID distribution status: In Commercial Distribution

Similar devices in this category

Other devices filed under Multiple drugs of abuse IVD, kit, rapid ICT, clinical.

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

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

Properties

Single use
Lot / batch number
Expiration date
Manufacturing date

Other properties (11, all answered No)