Catalog Number

DFUSTAPLERKIT

Brand Name

NA

Version/Model Number

DFUSTAPLERKIT

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"

Yes

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

GAG

Product Code Name

Stapler, Surgical

Public Device Record Key

a344a4d2-0f6c-4b4c-ae44-77bb5b0d0426

Public Version Date

October 26, 2022

Public Version Number

5

DI Record Publish Date

May 11, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-