Catalog Number

-

Brand Name

RITE AID

Version/Model Number

BP3NU1-3ERITE

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

69b5d114-8282-4efd-a0a0-6b50251caf6a

Public Version Date

January 17, 2022

Public Version Number

1

DI Record Publish Date

January 07, 2022

Package DI Number

10011822622353

Quantity per Package

12

Contains DI Package

00011822622356

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-