CARDINAL HEALTH - SHUNT RGH - Cardinal Health 200, LLC

Duns Number:961027315

Device Description: SHUNT RGH

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More Product Details

Catalog Number

SNE30SHRHH

Brand Name

CARDINAL HEALTH

Version/Model Number

SNE30SHRHH

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 19, 2017

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

OJG

Product Code Name

Neurological tray

Device Record Status

Public Device Record Key

7d65c25b-2a7e-4244-9143-cf6b1985703a

Public Version Date

July 17, 2018

Public Version Number

3

DI Record Publish Date

November 06, 2015

Additional Identifiers

Package DI Number

50887488376385

Quantity per Package

2

Contains DI Package

10887488376387

Package Discontinue Date

October 19, 2017

Package Status

Not in Commercial Distribution

Package Type

CASE

"CARDINAL HEALTH 200, LLC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 101686
2 A medical device with a moderate to high risk that requires special controls. 139430
3 A medical device with high risk that requires premarket approval 8
U Unclassified 40