Catalog Number

8881135084

Brand Name

Monoject

Version/Model Number

8881135084

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

79075a2a-04d0-423f-be4d-72abc5a279b0

Public Version Date

February 23, 2021

Public Version Number

7

DI Record Publish Date

September 24, 2016

Package DI Number

20884521010939

Quantity per Package

100

Contains DI Package

10884521010932

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE