Catalog Number

-

Brand Name

McKesson

Version/Model Number

1992

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"

Yes

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

c9a79929-1400-49f2-bf55-5a7a12215fcd

Public Version Date

November 08, 2019

Public Version Number

3

DI Record Publish Date

December 09, 2016

Package DI Number

40612479205282

Quantity per Package

100

Contains DI Package

10612479205274

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case