DrugCheck - DrugCheck NxStep OnSite Drug Test, - Express Diagnostic Int'l, Inc.

Duns Number:015875273

Device Description: DrugCheck NxStep OnSite Drug Test, AMP-BARB-BUP-BZO-COC-MET-MTD-OPI-OXY-PCP-PPX-TCA-THC

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More Product Details

Catalog Number

61329

Brand Name

DrugCheck

Version/Model Number

61329

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

Product Characteristics

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 Details

Product Code

DIO

Product Code Name

Enzyme Immunoassay, Cocaine And Cocaine Metabolites

Device Record Status

Public Device Record Key

628d1ebe-7237-49bb-9d77-6e6adffa1842

Public Version Date

June 10, 2022

Public Version Number

3

DI Record Publish Date

October 19, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"EXPRESS DIAGNOSTIC INT'L, INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 286
U Unclassified 2