Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

2110

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 09, 2021

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

FSM

Product Code Name

TRAY, SURGICAL, INSTRUMENT

Public Device Record Key

fc6653a0-dc90-4807-ac67-da46eb3717fa

Public Version Date

June 15, 2021

Public Version Number

5

DI Record Publish Date

August 20, 2016

Package DI Number

30809160003347

Quantity per Package

8

Contains DI Package

20809160003340

Package Discontinue Date

June 09, 2021

Package Status

Not in Commercial Distribution

Package Type

-