Catalog Number

-

Brand Name

VixOne

Version/Model Number

0236

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

7ecb2dff-0078-4bfa-96d8-c4cb7e167997

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

April 17, 2017

Package DI Number

10709078002332

Quantity per Package

50

Contains DI Package

00709078002335

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-