Catalog Number

-

Brand Name

BASNWS -30/150

Version/Model Number

BASNWS -30/150

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"

-

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

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

df80c115-5361-4b37-9257-a43ecc63212e

Public Version Date

September 24, 2019

Public Version Number

2

DI Record Publish Date

September 05, 2019

Package DI Number

10850005864568

Quantity per Package

50

Contains DI Package

00850005864561

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-