Identify®Diagnostics Drug Test Cups

Basic Information

• Brand Name: Identify®Diagnostics Drug Test Cups
• Primary DI: 10850013035615
• Version / Model: ID-US9-ADULT-6AM-1-AZ25
• Catalog Number: ID-US9-ADULT-6AM-1-AZ25
• Company Name: MEDICAL DISTRIBUTION GROUP INC
• Labeler DUNS: 064177324
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 25
• Record Status: Published
• Publish Date: 2026-03-24
• Public Version: 1
• Public Version Date: 2026-04-01
• Public Version Status: New
• Public Device Record Key: 09229e1e-27d2-4974-86d3-313f0522f9b3
• Distribution End Date: 2056-03-24

Device Description

Identify Diagnostics USA, 9 Panel Drug Screen Test Cup, CLIA Wavied (6AM10, AMP500, BAR300, BZO300, COC150, THC20, MTD300, MOP300, OXY100) + ( OX,pH,SG) + ( GL,NI,CR) Contents: Test Cups - 25, Package Insert - 1, Adulteration Card -1, Security Seals - 25, For In Vitro Diagnostics Use

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): Yes
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: Yes
• 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	Medical Specialty	Regulation #	Device Class
DJR	Enzyme Immunoassay, Methadone	Clinical Toxicology	862.3620	2
DIS	Enzyme Immunoassay, Barbiturate	Clinical Toxicology	862.3150	2
JXM	Enzyme Immunoassay, Benzodiazepine	Clinical Toxicology	862.3170	2
DIO	Enzyme Immunoassay, Cocaine And Cocaine Metabolites	Clinical Toxicology	862.3250	2
LDJ	Enzyme Immunoassay, Cannabinoids	Clinical Toxicology	862.3870	2
DKZ	Enzyme Immunoassay, Amphetamine	Clinical Toxicology	862.3100	2

GMDN Terms

Code	Name	Definition	Implantable	Status
46994	Multiple drugs of abuse IVD, kit, rapid ICT, clinical	A collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative detection of multiple drugs of abuse in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method [lateral flow test]. This is a rapid test used in the laboratory or in point-of-care analyses. It is not intended to be used for self-testing.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Unit of Use	00850013035991	GS1
Primary	10850013035615	GS1

Storage Conditions

• Type: Storage Environment Temperature
• Temperature Range: 2 – 30 Degrees Celsius