Catalog Number

9166017V

Brand Name

Injekt®

Version/Model Number

9166017V

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"

Yes

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

91bdd96f-85e5-4054-8b48-52e42bbc5e2e

Public Version Date

July 07, 2020

Public Version Number

5

DI Record Publish Date

September 23, 2016

Package DI Number

04022495252081

Quantity per Package

18

Contains DI Package

04022495252074

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton