Catalog Number

-

Brand Name

VIVE

Version/Model Number

SUP2019

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

49d87d4a-1d6a-4698-b38a-33fcd66dbf3c

Public Version Date

October 07, 2019

Public Version Number

2

DI Record Publish Date

September 23, 2019

Package DI Number

10818323029502

Quantity per Package

1

Contains DI Package

00818323029505

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case