Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

76845

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 11, 2018

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

Yes

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

OFF

Product Code Name

Central venous catheter tray

Public Device Record Key

09c7d14b-e612-4c16-8d62-8c3169abfac9

Public Version Date

October 06, 2020

Public Version Number

5

DI Record Publish Date

August 22, 2017

Package DI Number

20809160160319

Quantity per Package

20

Contains DI Package

10809160160312

Package Discontinue Date

December 11, 2018

Package Status

Not in Commercial Distribution

Package Type

-