Catalog Number

0250-282-059

Brand Name

NA

Version/Model Number

0250282059

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 15, 2019

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

-

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

3f9dae67-4d49-49ff-9afc-4ca43267d923

Public Version Date

August 21, 2019

Public Version Number

5

DI Record Publish Date

September 23, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-