Catalog Number

ID-CP12-AZ5

Brand Name

Identify Home Drug Testing Device Test Cups

Version/Model Number

ID-CP12-AZ5

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

DIO

Product Code Name

Enzyme Immunoassay, Cocaine And Cocaine Metabolites

Public Device Record Key

c2e03395-8c55-47d0-992f-cf5e1fa00fde

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

September 21, 2016

Package DI Number

20850721007345

Quantity per Package

40

Contains DI Package

10850721007348

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case