Catalog Number

-

Brand Name

equate

Version/Model Number

BP3KC1-3EWM

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

Yes

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

20967cbf-d824-48da-b200-4ca1d49103d7

Public Version Date

November 08, 2019

Public Version Number

3

DI Record Publish Date

September 10, 2018

Package DI Number

10681131247891

Quantity per Package

6

Contains DI Package

00681131247894

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton packing