Catalog Number

SLC5TLTSSC

Brand Name

CARDINAL HEALTH

Version/Model Number

SLC5TLTSSC

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

ace9be74-f012-4303-9af0-9f1788b30e02

Public Version Date

July 20, 2018

Public Version Number

3

DI Record Publish Date

April 07, 2016

Package DI Number

50885425833366

Quantity per Package

2

Contains DI Package

00885425833361

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE