Catalog Number

320-3NEO

Brand Name

Medicut™

Version/Model Number

320-3NEO

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

LRW

Product Code Name

Scissors, General, Surgical

Public Device Record Key

6d358304-392c-4ebf-af2c-19c38942950e

Public Version Date

March 19, 2021

Public Version Number

2

DI Record Publish Date

May 11, 2018

Package DI Number

00634782595371

Quantity per Package

18

Contains DI Package

00634782093952

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case