Catalog Number

4009

Brand Name

Urine Calibration Standard

Version/Model Number

4009

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

JIT

Product Code Name

Calibrator, Secondary

Public Device Record Key

72b5399b-a2b5-472e-b3ce-9cc86014372b

Public Version Date

April 09, 2019

Public Version Number

2

DI Record Publish Date

March 22, 2019

Package DI Number

04250317534323

Quantity per Package

5

Contains DI Package

04250317546333

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-