Catalog Number

-

Brand Name

VIVE

Version/Model Number

MOB1032

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

KNO

Product Code Name

Accessories, Wheelchair

Public Device Record Key

19c29031-b124-4641-b08a-d01fc163590b

Public Version Date

August 20, 2019

Public Version Number

1

DI Record Publish Date

August 12, 2019

Package DI Number

10818323028703

Quantity per Package

50

Contains DI Package

00818323028706

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case