Catalog Number

-

Brand Name

VIVE

Version/Model Number

SUP1013L

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

-

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

ILG

Product Code Name

Stocking, Elastic

Public Device Record Key

8ddafa96-3cd7-44d0-8719-1c44265be422

Public Version Date

August 30, 2022

Public Version Number

4

DI Record Publish Date

January 22, 2019

Package DI Number

10818323025924

Quantity per Package

40

Contains DI Package

00818323025927

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case