Catalog Number

-

Brand Name

Portex

Version/Model Number

C45091315J

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

-

Product Code

BSJ

Product Code Name

MASK, GAS, ANESTHETIC

Public Device Record Key

f0a7d5b5-3d62-4b56-8fa7-e8e87829d667

Public Version Date

October 24, 2022

Public Version Number

4

DI Record Publish Date

January 03, 2017

Package DI Number

30351688433385

Quantity per Package

20

Contains DI Package

00351688433384

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CARTON