Catalog Number

-

Brand Name

RAP Femoral Venous Cannula

Version/Model Number

200-150

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

K052081,K052081

Product Code

DWF

Product Code Name

CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

Public Device Record Key

12ce1201-57ba-4e7b-ac0f-7386eb90c147

Public Version Date

August 15, 2018

Public Version Number

4

DI Record Publish Date

September 17, 2015

Package DI Number

10803622128094

Quantity per Package

1

Contains DI Package

00803622128097

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE