CARDINAL HEALTH - KIT,NEURO - Cardinal Health 200, LLC

Duns Number:961027315

Device Description: KIT,NEURO

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More Product Details

Catalog Number

PNHDNJHUG

Brand Name

CARDINAL HEALTH

Version/Model Number

PNHDNJHUG

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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

3cc4a8d7-884b-42ba-8de2-0e5ab9c86c4d

Public Version Date

May 15, 2020

Public Version Number

1

DI Record Publish Date

May 07, 2020

Additional Identifiers

Package DI Number

50888439494172

Quantity per Package

1

Contains DI Package

10888439494174

Package Discontinue Date

-

Package Status

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