Catalog Number

01721

Brand Name

Not Applicable

Version/Model Number

#172

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

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

GES

Product Code Name

Blade, Scalpel

Public Device Record Key

bcc41121-c26c-4300-8236-0751f5149f5a

Public Version Date

January 22, 2021

Public Version Number

3

DI Record Publish Date

July 01, 2020

Package DI Number

58904233117214

Quantity per Package

10000

Contains DI Package

18904233117216

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton