Catalog Number

-

Brand Name

DPS

Version/Model Number

3ml

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

52459ec6-0a37-44f1-9121-c2d663585231

Public Version Date

December 25, 2020

Public Version Number

1

DI Record Publish Date

December 17, 2020

Package DI Number

16935550810056

Quantity per Package

100

Contains DI Package

06935550810059

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box