Catalog Number

-

Brand Name

Circulaire Aerosol Drug Delivery System

Version/Model Number

0321

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

1ba4e0f2-5302-4223-9422-1df195bb04a2

Public Version Date

November 19, 2020

Public Version Number

4

DI Record Publish Date

December 11, 2016

Package DI Number

10709078000857

Quantity per Package

25

Contains DI Package

00709078000850

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-