Catalog Number

0703-047-005

Brand Name

Stryker

Version/Model Number

0703-047-005

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

GEI

Product Code Name

Electrosurgical, cutting & coagulation & accessories

Public Device Record Key

1344b89b-d1e1-46a2-9274-35dfa5be6edf

Public Version Date

April 06, 2020

Public Version Number

4

DI Record Publish Date

October 15, 2019

Package DI Number

37613327467650

Quantity per Package

10

Contains DI Package

07613327467659

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

pack