Catalog Number

DP5050

Brand Name

C I P M DiscPoint™ Fluid Dispensing Syringe

Version/Model Number

QL20120

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

DXT

Product Code Name

Injector And Syringe, Angiographic

Public Device Record Key

b1362d19-e3dd-4944-9487-45c53d1f3a7f

Public Version Date

November 05, 2020

Public Version Number

4

DI Record Publish Date

September 20, 2016

Package DI Number

10856877002572

Quantity per Package

5

Contains DI Package

00856877002575

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-