Catalog Number

BB1000LF

Brand Name

CARDINAL HEALTH

Version/Model Number

BB1000LF

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"

Yes

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

BTC

Product Code Name

BAG, RESERVOIR

Public Device Record Key

183e7dfa-bf05-407d-bc0c-72b7bfcb760c

Public Version Date

January 21, 2019

Public Version Number

1

DI Record Publish Date

December 19, 2018

Package DI Number

50885380063839

Quantity per Package

30

Contains DI Package

10885380063831

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE