Catalog Number

768-619-11ANKIT

Brand Name

Pro's Combo™

Version/Model Number

768-619-11ANKIT

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

a388079b-daec-4bf8-ad0d-1cf3e3f2de68

Public Version Date

August 09, 2021

Public Version Number

1

DI Record Publish Date

July 30, 2021

Package DI Number

00634782599348

Quantity per Package

3

Contains DI Package

00634782097967

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case