Catalog Number

7302T

Brand Name

Express™

Version/Model Number

7302T

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

ELW

Product Code Name

MATERIAL, IMPRESSION

Public Device Record Key

0bbb0f66-b5b6-4274-8da9-1a69109e1271

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

July 24, 2017

Package DI Number

50605861036073

Quantity per Package

5

Contains DI Package

30605861036079

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX