Catalog Number

-

Brand Name

MEDI

Version/Model Number

2990002

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 19, 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"

-

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

FQJ

Product Code Name

SUPPORT, SCROTAL, THERAPEUTIC

Public Device Record Key

4c5ea44f-abfc-4096-922b-71117f53ab1b

Public Version Date

May 20, 2020

Public Version Number

2

DI Record Publish Date

January 08, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-