Catalog Number

-

Brand Name

CathGrip

Version/Model Number

51250NSLA

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

Yes

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

KMK

Product Code Name

Device, Intravascular Catheter Securement

Public Device Record Key

96bbf420-8ded-4d93-ad29-10f470d8f0f7

Public Version Date

August 24, 2021

Public Version Number

1

DI Record Publish Date

August 16, 2021

Package DI Number

10653599001438

Quantity per Package

30

Contains DI Package

00653599001431

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box