Catalog Number

-

Brand Name

Moore Medical

Version/Model Number

13786

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

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

CDM

Product Code Name

Diazonium Colorimetry, Urobilinogen (Urinary, Non-Quant.)

Public Device Record Key

a38bc4a5-a5e3-4d3f-8177-06f895e86a2a

Public Version Date

October 31, 2022

Public Version Number

5

DI Record Publish Date

December 09, 2016

Package DI Number

40607415001301

Quantity per Package

1

Contains DI Package

10607415001294

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case