Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

56786

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

March 15, 2017

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

MMO

Product Code Name

TRAY, SURGICAL, ENT

Public Device Record Key

08435723-9e04-4d90-b19f-f3d50ff66bef

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

August 20, 2016

Package DI Number

20809160023669

Quantity per Package

20

Contains DI Package

10809160023662

Package Discontinue Date

March 15, 2017

Package Status

Not in Commercial Distribution

Package Type

-