Catalog Number

NGF03-11023180

Brand Name

NA

Version/Model Number

NGF03-11023180

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

OCZ

Product Code Name

Endoscopic Grasping/Cutting Instrument, Non-Powered

Public Device Record Key

37901397-d2df-4cab-9bdd-62d10bd34327

Public Version Date

May 17, 2021

Public Version Number

4

DI Record Publish Date

March 11, 2016

Package DI Number

26932503561017

Quantity per Package

10

Contains DI Package

16932503561010

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case