Catalog Number

-

Brand Name

INSPIRE

Version/Model Number

8 PH.I.S.I.O.

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

DTZ

Product Code Name

OXYGENATOR, CARDIOPULMONARY BYPASS

Public Device Record Key

b69ec55e-70fd-4dbf-b20f-2fb7e037c93b

Public Version Date

January 22, 2020

Public Version Number

3

DI Record Publish Date

May 13, 2015

Package DI Number

38033178112360

Quantity per Package

2

Contains DI Package

08033178112369

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX