Catalog Number

203887S

Brand Name

Terumo Cardiovascular Systems

Version/Model Number

203887S

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

dc19ca44-53b9-42a0-b2e9-3fdcd8ca6aa9

Public Version Date

September 21, 2022

Public Version Number

5

DI Record Publish Date

September 23, 2016

Package DI Number

10817278011440

Quantity per Package

10

Contains DI Package

00817278011443

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case