NexScreen Cup - CLIA-waived NexScreen Cup - NEXSCREEN, LLC

Duns Number:031433133

Device Description: CLIA-waived NexScreen Cup 12AMP1000/BAR300/BZO300/COC300/MDMA500/MET1000/MTD300/OPI300/OXY CLIA-waived NexScreen Cup 12AMP1000/BAR300/BZO300/COC300/MDMA500/MET1000/MTD300/OPI300/OXY100/PCP25/TCA1000/THC50

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More Product Details

Catalog Number

NXS-61203N

Brand Name

NexScreen Cup

Version/Model Number

NXS-61203N

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)

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

daf3fdca-45ca-45b4-beb6-792610fbe80b

Public Version Date

June 10, 2022

Public Version Number

3

DI Record Publish Date

August 30, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"NEXSCREEN, LLC" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 34