Catalog Number

-

Brand Name

Disposable Insulin Syringe

Version/Model Number

U-100 0.5ML 30G×8mm No protective end top

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)

-

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

67ba1a2d-6a5a-44cd-b9b7-765fe8caf654

Public Version Date

January 20, 2020

Public Version Number

4

DI Record Publish Date

March 31, 2017

Package DI Number

06949236201802

Quantity per Package

30

Contains DI Package

06949236200768

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-