Catalog Number

-

Brand Name

Olympus

Version/Model Number

WA98500A

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

GEI

Product Code Name

Electrosurgical, Cutting & Coagulation & Accessories

Public Device Record Key

5dae2418-3af6-4fbc-957f-6c7b17a579b6

Public Version Date

April 26, 2018

Public Version Number

1

DI Record Publish Date

March 26, 2018

Package DI Number

36939029817533

Quantity per Package

2

Contains DI Package

26939029817536

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton