Identify® Diagnostics Drug Test Cards - Identify® Diagnostics Drug Test Cards 12 Panel - MEDICAL DISTRIBUTION GROUP INC

Duns Number:064177324

Device Description: Identify® Diagnostics Drug Test Cards 12 Panel Drug Test Card THC/COC/MOP/OXY/MDMA/BUP/AMP Identify® Diagnostics Drug Test Cards 12 Panel Drug Test Card THC/COC/MOP/OXY/MDMA/BUP/AMP/BAR/BZO/MET/MTD/PCP

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More Product Details

Catalog Number

ID-CP12-DIP-AZ25

Brand Name

Identify® Diagnostics Drug Test Cards

Version/Model Number

ID-CP12-DIP-AZ25

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K131811,K131811,K131811

Product Code Details

Product Code

DIO

Product Code Name

Enzyme Immunoassay, Cocaine And Cocaine Metabolites

Device Record Status

Public Device Record Key

18bae41c-0a4b-4a19-aaef-487404fd1d7a

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

February 26, 2018

Additional Identifiers

Package DI Number

20850721007697

Quantity per Package

40

Contains DI Package

10850721007690

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case

"MEDICAL DISTRIBUTION GROUP INC" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 8