Catalog Number

-

Brand Name

VIVE

Version/Model Number

MOB1014BLK

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

IPR

Product Code Name

Crutch

Public Device Record Key

68f87532-0660-4491-994b-5a11c46c0e94

Public Version Date

March 25, 2019

Public Version Number

1

DI Record Publish Date

March 17, 2019

Package DI Number

10818323027195

Quantity per Package

10

Contains DI Package

00818323027198

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case