Catalog Number

-

Brand Name

HEB in Control

Version/Model Number

BP3MD1-HEB

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

DXN

Product Code Name

System, Measurement, Blood-Pressure, Non-Invasive

Public Device Record Key

532ad8a5-255b-48fe-8653-84537387583a

Public Version Date

November 08, 2019

Public Version Number

3

DI Record Publish Date

November 21, 2016

Package DI Number

10041220800411

Quantity per Package

6

Contains DI Package

00041220800414

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton packing