Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

73564

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FNY

Product Code Name

BASIN, EMESIS

Public Device Record Key

c56faecb-71a5-43ab-b393-7f36f3064b89

Public Version Date

October 29, 2021

Public Version Number

4

DI Record Publish Date

August 20, 2016

Package DI Number

20809160018832

Quantity per Package

8

Contains DI Package

10809160018835

Package Discontinue Date

March 12, 2020

Package Status

Not in Commercial Distribution

Package Type

-