Catalog Number

-

Brand Name

MH

Version/Model Number

3012

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FXP

Product Code Name

Cover, Shoe, Operating-Room

Public Device Record Key

9a7efb92-e526-4870-b505-237cf6d24a13

Public Version Date

April 07, 2021

Public Version Number

2

DI Record Publish Date

September 15, 2020

Package DI Number

10850018327692

Quantity per Package

3

Contains DI Package

00850018327695

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case