Catalog Number

701047379

Brand Name

Tubing Pack

Version/Model Number

BEQ TOP 15800

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 05, 2018

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)

Yes

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

DWE

Product Code Name

Tubing, Pump, Cardiopulmonary Bypass

Public Device Record Key

e9ee4739-09a3-45d3-8e3c-a1c24b611671

Public Version Date

December 02, 2019

Public Version Number

5

DI Record Publish Date

January 29, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-