Catalog Number

-

Brand Name

MEDICAL ACTION INDUSTRIES

Version/Model Number

79522

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 12, 2020

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

PEV

Product Code Name

Dialysis administration kit

Public Device Record Key

ca446379-c5c3-4cb5-80e9-fc77d5c1ab9b

Public Version Date

May 13, 2020

Public Version Number

2

DI Record Publish Date

August 19, 2019

Package DI Number

20809160254001

Quantity per Package

20

Contains DI Package

10809160254004

Package Discontinue Date

May 12, 2020

Package Status

Not in Commercial Distribution

Package Type

-