Catalog Number

8881520178

Brand Name

Monoject

Version/Model Number

8881520178

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

July 01, 2023

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

cb08dc36-fc94-4482-a33b-872b58ff4970

Public Version Date

October 11, 2021

Public Version Number

6

DI Record Publish Date

September 24, 2016

Package DI Number

40884521012135

Quantity per Package

40

Contains DI Package

10884521012134

Package Discontinue Date

July 01, 2023

Package Status

In Commercial Distribution

Package Type

PACK_OR_INNER_PACK