Catalog Number

-

Brand Name

Portex

Version/Model Number

11-1030

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

CAF

Product Code Name

NEBULIZER (DIRECT PATIENT INTERFACE)

Public Device Record Key

fc2a4afd-8441-4d59-8924-533e4d3145cb

Public Version Date

March 23, 2020

Public Version Number

3

DI Record Publish Date

October 11, 2016

Package DI Number

50788942110302

Quantity per Package

25

Contains DI Package

10788942110304

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE