Catalog Number

-

Brand Name

Portex

Version/Model Number

C45101762

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"

Yes

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

CAH

Product Code Name

Filter, bacterial, breathing-circuit

Public Device Record Key

d65e551c-d18e-46d0-893f-48cef14b778b

Public Version Date

October 24, 2022

Public Version Number

4

DI Record Publish Date

July 05, 2016

Package DI Number

25019517036470

Quantity per Package

20

Contains DI Package

15019517036473

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX