CARDINAL HEALTH - SAFETY BM BIOPSY NO NEEDLE PK - Cardinal Health 200, LLC

Duns Number:961027315

Device Description: SAFETY BM BIOPSY NO NEEDLE PK

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More Product Details

Catalog Number

31-BM4SF

Brand Name

CARDINAL HEALTH

Version/Model Number

31-BM4SF

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

GAA

Product Code Name

NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE

Device Record Status

Public Device Record Key

5f72987a-9f07-43fa-bb99-b3515c9606d6

Public Version Date

July 19, 2018

Public Version Number

3

DI Record Publish Date

January 17, 2017

Additional Identifiers

Package DI Number

50885425210297

Quantity per Package

10

Contains DI Package

10885425210299

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