Catalog Number

CP3020R

Brand Name

ChemoPlus

Version/Model Number

CP3020R

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

-

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

KPE

Product Code Name

CONTAINER, I.V.

Public Device Record Key

c35c28ce-fa68-4cc5-a168-368eeeb62ec2

Public Version Date

November 08, 2021

Public Version Number

8

DI Record Publish Date

September 24, 2016

Package DI Number

20884527006332

Quantity per Package

12000

Contains DI Package

10884527006335

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE