Catalog Number

-

Brand Name

Sunmark

Version/Model Number

BPMU1-2ESMARK

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

f13676c6-1e70-49ed-a835-d196711b2dcc

Public Version Date

June 11, 2020

Public Version Number

4

DI Record Publish Date

December 30, 2016

Package DI Number

10038703919067

Quantity per Package

12

Contains DI Package

00038703919060

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton packing