Catalog Number

JGLUT

Brand Name

Crosstex International

Version/Model Number

JGLUT

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

MED

Product Code Name

Sterilant, medical devices

Public Device Record Key

e6d89457-47fc-447b-9322-c6b5ce2eab8c

Public Version Date

March 19, 2021

Public Version Number

5

DI Record Publish Date

November 11, 2016

Package DI Number

50732224000119

Quantity per Package

4

Contains DI Package

10732224000111

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-