Catalog Number

-

Brand Name

VIVE

Version/Model Number

MOB1029

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)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

ITI

Product Code Name

Wheelchair, Powered

Public Device Record Key

e7f9ae9d-1fd3-4446-b539-4943d8f3590f

Public Version Date

June 11, 2019

Public Version Number

1

DI Record Publish Date

June 03, 2019

Package DI Number

10818323028024

Quantity per Package

1

Contains DI Package

00818323028027

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case