Catalog Number

701049513

Brand Name

Small Patient ECC Pack

Version/Model Number

BEQ-TOP 22301

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

97ac3464-0e77-46c0-a6c6-7cbcdffe3bee

Public Version Date

December 02, 2019

Public Version Number

5

DI Record Publish Date

February 14, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-