Identify ® Diagnostics Drug Test Cups 12-Panel Drug Screening Test Cup - Identify ® Diagnostics Drug Test Cups 12-Panel - MEDICAL DISTRIBUTION GROUP INC

Duns Number:064177324

Device Description: Identify ® Diagnostics Drug Test Cups 12-Panel Drug Screening Test Cup AMP/BAR/BUP/BZO/COC Identify ® Diagnostics Drug Test Cups 12-Panel Drug Screening Test Cup AMP/BAR/BUP/BZO/COC/EDDP/MDMA/MET/MOP/MTD/OXY/THC

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More Product Details

Catalog Number

ID-CP12-EDDP

Brand Name

Identify ® Diagnostics Drug Test Cups 12-Panel Drug Screening Test Cup

Version/Model Number

ID-CP12-EDDP

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

-

Product Code Details

Product Code

DIO

Product Code Name

Enzyme Immunoassay, Cocaine And Cocaine Metabolites

Device Record Status

Public Device Record Key

55087a6a-e18a-4ec8-8dbd-9593b9991c8d

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

February 18, 2017

Additional Identifiers

Package DI Number

20850721007406

Quantity per Package

8

Contains DI Package

10850721007409

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