Catalog Number

7873

Brand Name

POREX SQ-EASY

Version/Model Number

Tube

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

LXG

Product Code Name

Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use

Public Device Record Key

f58546d2-c0d7-4012-a44e-18aaf83cb841

Public Version Date

January 22, 2021

Public Version Number

3

DI Record Publish Date

June 11, 2018

Package DI Number

20817139020755

Quantity per Package

5

Contains DI Package

10817139020758

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-