Catalog Number

731-MCC1

Brand Name

Multikuf™

Version/Model Number

731-MCC1

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

DXQ

Product Code Name

Blood Pressure Cuff

Public Device Record Key

3e0db417-5492-4a8a-8267-bc3d27fd1b3f

Public Version Date

September 07, 2020

Public Version Number

1

DI Record Publish Date

August 29, 2020

Package DI Number

00634782597801

Quantity per Package

5

Contains DI Package

00634782096427

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case