Catalog Number

0250080619

Brand Name

NA

Version/Model Number

0250080619

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

-

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

08104725-d556-48e0-a35d-6ff4e74491af

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 23, 2016

Package DI Number

37613327058650

Quantity per Package

5

Contains DI Package

07613327058659

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

pack