Catalog Number

-

Brand Name

Single Use Injector NM600/610

Version/Model Number

NM-600L-0423

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 18, 2022

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

FBK

Product Code Name

endoscopic injection needle, gastroenterology-urology

Public Device Record Key

3de02772-21d8-48e1-bcf0-c8b30752a797

Public Version Date

August 19, 2022

Public Version Number

4

DI Record Publish Date

September 16, 2020

Package DI Number

14953170422703

Quantity per Package

5

Contains DI Package

04953170422706

Package Discontinue Date

August 18, 2022

Package Status

Not in Commercial Distribution

Package Type

-