FDA UDI In Commercial Distribution 🇺🇸 United States

Identify Diagnostics Multi-Drug Rapid Test Cup

DI: 16942598228378 · Model: 1 · Hangzhou AllTest Biotech Co., Ltd.
Product Codes
5
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

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Basic Information

Brand Name
Identify Diagnostics Multi-Drug Rapid Test Cup
Primary DI
16942598228378
Version / Model
1
Catalog Number
DOA-A167C
Company Name
Hangzhou AllTest Biotech Co., Ltd.
Labeler DUNS
543254717
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2026-04-02
Public Version
1
Public Version Date
2026-04-10
Public Version Status
New
Public Device Record Key
2a765cc5-f296-4b60-a57c-8c75e9434daa

Device Description

25T, EN, non-CE,AMP1000/BZO300/COC300/MOP300/OXY100/THC50

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
NFT Test, Amphetamine, Over The Counter
NGL Test, Opiates, Over The Counter
NFY Test, Cocaine And Cocaine Metabolites, Over The Counter
NFW Test, Cannabinoid, Over The Counter
NFV Test, Benzodiazepine, Over The Counter

GMDN Terms

Code Name
46994 Multiple drugs of abuse IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Unit of Use 06942598228371
Primary 16942598228378