Catalog Number

-

Brand Name

CP-xxxxx

Version/Model Number

CP-xxxxx

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

DWF

Product Code Name

CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

Public Device Record Key

f0a415c7-55e4-460f-b01b-fee0e3e1787b

Public Version Date

August 15, 2018

Public Version Number

3

DI Record Publish Date

July 16, 2015

Package DI Number

10803622126755

Quantity per Package

10

Contains DI Package

00803622126758

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE