Catalog Number

SLC30LPQCA

Brand Name

CARDINAL HEALTH

Version/Model Number

SLC30LPQCA

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 24, 2017

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

06fa3daa-bd8d-4b8b-acee-72553ae5e848

Public Version Date

July 20, 2018

Public Version Number

3

DI Record Publish Date

July 21, 2015

Package DI Number

50885425912801

Quantity per Package

16

Contains DI Package

00885425912806

Package Discontinue Date

October 24, 2017

Package Status

Not in Commercial Distribution

Package Type

CASE