Catalog Number

-

Brand Name

DRI 50 mg/dL Alcohol Control

Version/Model Number

0239

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

DKC

Product Code Name

Alcohol Control Materials

Public Device Record Key

4b6d3abe-19a9-400b-a3cb-baf1f3235717

Public Version Date

April 24, 2019

Public Version Number

4

DI Record Publish Date

October 30, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-