Catalog Number

SNE51GNSFE

Brand Name

CARDINAL HEALTH

Version/Model Number

SNE51GNSFE

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

OJG

Product Code Name

Neurological tray

Public Device Record Key

9c1517b0-08be-4bb0-940d-740609c45c11

Public Version Date

July 17, 2018

Public Version Number

3

DI Record Publish Date

August 31, 2015

Package DI Number

50887488037446

Quantity per Package

3

Contains DI Package

00887488037441

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE