Catalog Number

-

Brand Name

MediChoice

Version/Model Number

ES3502

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

FME

Product Code Name

Gown, examination

Public Device Record Key

a11c65cb-b019-4e92-b42e-2004099cda9e

Public Version Date

March 11, 2021

Public Version Number

1

DI Record Publish Date

March 03, 2021

Package DI Number

30885632291153

Quantity per Package

4

Contains DI Package

20885632291156

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-