Catalog Number

-

Brand Name

DPS

Version/Model Number

1ml

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

f49227ee-43d8-4452-b5a5-aed49fe7cac7

Public Version Date

December 07, 2020

Public Version Number

1

DI Record Publish Date

November 27, 2020

Package DI Number

16935550810018

Quantity per Package

100

Contains DI Package

06935550810011

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box