Ten Panel PreScreen Plus Cup With Adulterants (CLIA Waived) - Ten Panel PreScreen Plus Cup With Adulterants - MERGERS MARKETING, INC.

Duns Number:065602744

Device Description: Ten Panel PreScreen Plus Cup With Adulterants (CLIA Waived) Drug Combo: AMP BAR BZO Ten Panel PreScreen Plus Cup With Adulterants (CLIA Waived) Drug Combo: AMP BAR BZO COC MDMA MET MTD OPI PCP THC + AD

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More Product Details

Catalog Number

-

Brand Name

Ten Panel PreScreen Plus Cup With Adulterants (CLIA Waived)

Version/Model Number

PSC-DOA-3104AD

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"

-

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

dae36946-f284-4ae0-9acd-ad7bd84f6bd0

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

July 25, 2016

Additional Identifiers

Package DI Number

00850557007577

Quantity per Package

25

Contains DI Package

00850557007560

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Pack

"MERGERS MARKETING, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1
2 A medical device with a moderate to high risk that requires special controls. 23