Catalog Number

3410Q

Brand Name

ADC®

Version/Model Number

3410Q

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

3ff95412-cb9e-4697-90d9-1021559be0df

Public Version Date

September 23, 2022

Public Version Number

4

DI Record Publish Date

September 21, 2016

Package DI Number

00634782536381

Quantity per Package

6

Contains DI Package

00634782836382

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case