Catalog Number

81025-EI

Brand Name

DrugCheck

Version/Model Number

81025-EI

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

PUX

Product Code Name

Test, Amphetamine, Employment And Insurance Testing, Exempt

Public Device Record Key

9f527816-daff-496d-8f3a-f4dca19084c0

Public Version Date

June 10, 2022

Public Version Number

3

DI Record Publish Date

March 12, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-