Catalog Number

SBA41BLGDC

Brand Name

CARDINAL HEALTH

Version/Model Number

SBA41BLGDC

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

FDE

Product Code Name

laparoscopy kit

Public Device Record Key

304efed8-46ba-4c8b-b80a-0654b25f359f

Public Version Date

November 04, 2020

Public Version Number

1

DI Record Publish Date

October 27, 2020

Package DI Number

50888439924334

Quantity per Package

2

Contains DI Package

10888439924336

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE