Catalog Number

IAB-05830-LWS

Brand Name

ARROW

Version/Model Number

IPN038101

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

DSP

Product Code Name

System, balloon, intra-aortic and control

Public Device Record Key

f508e586-e310-4d17-9ab6-5ca2560bb165

Public Version Date

January 18, 2021

Public Version Number

3

DI Record Publish Date

December 04, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-