CARDINAL HEALTH - BLOCK SPINAL KIT - Cardinal Health 200, LLC

Duns Number:961027315

Device Description: BLOCK SPINAL KIT

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More Product Details

Catalog Number

17A4091C

Brand Name

CARDINAL HEALTH

Version/Model Number

17A4091C

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

OFU

Product Code Name

Spinal anesthesia kit

Device Record Status

Public Device Record Key

1253415d-96ca-4688-a19c-8ed3c558cf5e

Public Version Date

August 30, 2018

Public Version Number

1

DI Record Publish Date

July 30, 2018

Additional Identifiers

Package DI Number

50888439039311

Quantity per Package

50

Contains DI Package

10888439039313

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