Catalog Number

-

Brand Name

BISON

Version/Model Number

DBP-1332

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

DXN

Product Code Name

System, Measurement, Blood-Pressure, Non-Invasive

Public Device Record Key

f74e48d8-ba5c-423c-8da3-1766381d1544

Public Version Date

November 08, 2019

Public Version Number

2

DI Record Publish Date

January 30, 2019

Package DI Number

10811787031319

Quantity per Package

24

Contains DI Package

00811787031312

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-