Catalog Number

-

Brand Name

Portex

Version/Model Number

100/131/070

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K931735,K931735,K931735

Product Code

BTR

Product Code Name

Tube, tracheal (w/wo connector)

Public Device Record Key

e2c25dd8-9e3d-4d8c-ad17-99c2db1f0932

Public Version Date

June 19, 2020

Public Version Number

5

DI Record Publish Date

September 01, 2015

Package DI Number

55019315057234

Quantity per Package

10

Contains DI Package

35019315057230

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case