Catalog Number

DP5201V

Brand Name

ChemoPlus

Version/Model Number

DP5201V

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

FMF

Product Code Name

Syringe, piston

Public Device Record Key

c0e9623d-f999-4d1d-95ec-a57dddaedfa7

Public Version Date

March 29, 2021

Public Version Number

8

DI Record Publish Date

September 24, 2016

Package DI Number

00884527004228

Quantity per Package

50

Contains DI Package

20884527004222

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

PACK_OR_INNER_PACK