Catalog Number

-

Brand Name

Vive Precision

Version/Model Number

DMD1038GRYL

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

DXQ

Product Code Name

Blood Pressure Cuff

Public Device Record Key

18ad14c8-24b7-4474-a2c9-858ee79e5b40

Public Version Date

July 22, 2019

Public Version Number

2

DI Record Publish Date

September 13, 2018

Package DI Number

10818323024613

Quantity per Package

80

Contains DI Package

00818323024616

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case