FDA UDI In Commercial Distribution 🇺🇸 United States

Rite Aid

DI: 00011822001663 · Model: 8024510 · RITE AID CORPORATION
Product Codes
4
GMDN Terms
4
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Rite Aid
Primary DI
00011822001663
Version / Model
8024510
Company Name
RITE AID CORPORATION
Labeler DUNS
014578892
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-29
Public Version
1
Public Version Date
2025-02-06
Public Version Status
New
Public Device Record Key
77554b39-74a3-4b93-9cfb-5951799b1d19

Device Description

Home Drug Test 4 Panel COC/OPI/mAMP/THC

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NFY Test, Cocaine And Cocaine Metabolites, Over The Counter
NGL Test, Opiates, Over The Counter
NGG Test, Methamphetamine, Over The Counter
NFW Test, Cannabinoid, Over The Counter

GMDN Terms

Code Name
55501 Methamphetamine-specific IVD, reagent
55553 Cannabinoid/cannabinoid metabolite IVD, reagent
55570 Cocaine/cocaine metabolite IVD, reagent
55724 Opiate/opiate metabolite IVD, reagent

Identifiers

Type ID
Primary 00011822001663