Catalog Number

CV9025

Brand Name

Kendall

Version/Model Number

CV9025

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

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

LKB

Product Code Name

Pad, alcohol, device disinfectant

Public Device Record Key

865a4706-656f-4486-ad29-1d995010d8f3

Public Version Date

August 07, 2020

Public Version Number

3

DI Record Publish Date

June 29, 2018

Package DI Number

30884521183661

Quantity per Package

2400

Contains DI Package

10884521183667

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE