Catalog Number

-

Brand Name

TERUFLEX TRANSFER BAG

Version/Model Number

BB*T200BB71

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

KSR

Product Code Name

Container, Empty, For Collection & Processing Of Blood & Blood Components

Public Device Record Key

23466978-fb75-40e4-b405-88280590e177

Public Version Date

June 17, 2022

Public Version Number

3

DI Record Publish Date

September 15, 2016

Package DI Number

54987350704615

Quantity per Package

4

Contains DI Package

34987350704611

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton