Catalog Number

-

Brand Name

MEDI

Version/Model Number

02555

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"

-

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

FQL

Product Code Name

STOCKING, MEDICAL SUPPORT (FOR GENERAL MEDICAL PURPOSES)

Public Device Record Key

4b08df1d-faa2-45fc-8543-cadcdd2bc462

Public Version Date

July 07, 2020

Public Version Number

4

DI Record Publish Date

January 02, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-