Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

81394

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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

LRS

Product Code Name

I.V. start kit

Public Device Record Key

ef3bafbb-953f-40f0-91ed-c4cc65c7798a

Public Version Date

April 07, 2021

Public Version Number

2

DI Record Publish Date

August 04, 2020

Package DI Number

20809160289133

Quantity per Package

30

Contains DI Package

10809160289136

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-