Catalog Number

-

Brand Name

VIVE

Version/Model Number

MOB1023BLK

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

IPS

Product Code Name

Cane

Public Device Record Key

dd104e7f-e2d5-4866-866e-c9d3d94ce71e

Public Version Date

April 01, 2019

Public Version Number

1

DI Record Publish Date

March 24, 2019

Package DI Number

10818323027317

Quantity per Package

8

Contains DI Package

00818323027310

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case