Catalog Number

BANPN1020S

Brand Name

BREEZE® APD

Version/Model Number

BANPN1020S

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

FGE

Product Code Name

Stents, drains and dilators for the biliary ducts

Public Device Record Key

cd082506-dafa-4c48-bb88-53edb3016153

Public Version Date

March 07, 2022

Public Version Number

1

DI Record Publish Date

February 26, 2022

Package DI Number

30884908138925

Quantity per Package

5

Contains DI Package

00884908138924

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

inner box