Catalog Number

760IHOP

Brand Name

Hopkins

Version/Model Number

760IHOP

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

DXQ

Product Code Name

Blood Pressure Cuff

Public Device Record Key

ec055ac8-1cc3-450e-a6c2-bd32b8d4bfac

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

July 21, 2017

Package DI Number

00634782532048

Quantity per Package

20

Contains DI Package

00634782032128

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case