Catalog Number

-

Brand Name

CathGrip

Version/Model Number

51250NSNA-4

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

a0c89716-a518-4515-bce0-a23e56581492

Public Version Date

July 01, 2022

Public Version Number

1

DI Record Publish Date

June 23, 2022

Package DI Number

10653599001827

Quantity per Package

75

Contains DI Package

00653599001820

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box