Catalog Number

-

Brand Name

microlife

Version/Model Number

BP3AQ1-1

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

688b9b54-9d6f-4370-a4e9-61346a0286d9

Public Version Date

November 08, 2019

Public Version Number

3

DI Record Publish Date

January 06, 2017

Package DI Number

10642632410092

Quantity per Package

12

Contains DI Package

00642632410095

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton packing