FDA UDI In Commercial Distribution 🇺🇸 United States

Alltest Multi-Drug Rapid Urine Test Panel

DI: 16936983169599 · Model: 1 · Hangzhou AllTest Biotech Co., Ltd.
Product Codes
10
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

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Basic Information

Brand Name
Alltest Multi-Drug Rapid Urine Test Panel
Primary DI
16936983169599
Version / Model
1
Catalog Number
DOA-A1144C-026-b
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
2026-04-15
Public Version
1
Public Version Date
2026-04-23
Public Version Status
New
Public Device Record Key
ef214896-83b7-43e8-a1e6-81677d6b7943

Device Description

25T/Box, FDA Clia Waived, MOP300/OXY100/PCP25/MET500/MDMA500/MTD300/AMP500/BAR300/BZO300/COC150/THC50/TCA1000/BUP10/FYL1

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
NFW Test, Cannabinoid, Over The Counter
NFT Test, Amphetamine, Over The Counter
NGL Test, Opiates, Over The Counter
NGG Test, Methamphetamine, Over The Counter
NGM Test, Phencyclidine (Pcp), Over The Counter
QAW Test, Tricyclic Antidepressants, Over The Counter
PTG Test, Methadone, Over The Counter
PTH Test, Barbiturate, 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 06936983169592
Primary 16936983169599