Catalog Number

-

Brand Name

VIVE

Version/Model Number

SUP1061

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

MHW

Product Code Name

Dressing, Compression

Public Device Record Key

bffa7fa3-c140-4155-874f-9e4e1d911399

Public Version Date

March 19, 2020

Public Version Number

1

DI Record Publish Date

March 11, 2020

Package DI Number

10810041981599

Quantity per Package

100

Contains DI Package

00810041981592

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case