Catalog Number

BUNS-1L

Brand Name

JAS Diagnostics

Version/Model Number

BUNS-1L

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

CDQ

Product Code Name

Urease And Glutamic Dehydrogenase, Urea Nitrogen

Public Device Record Key

fd78bc0f-0a3a-4f5d-99e7-25083e400182

Public Version Date

May 28, 2018

Public Version Number

1

DI Record Publish Date

April 26, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-