Catalog Number

631

Brand Name

Pantex Universal

Version/Model Number

1 Universal

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

NHG

Product Code Name

Enzyme Immunoassay, Cortisol, Salivary

Public Device Record Key

8dcdfbdf-e67b-4c61-bef2-5073412a6580

Public Version Date

May 31, 2022

Public Version Number

1

DI Record Publish Date

May 23, 2022

Package DI Number

10850039602150

Quantity per Package

1

Contains DI Package

00850039602153

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton Box