Catalog Number

-

Brand Name

Olympus

Version/Model Number

WA98230B

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

479b2a33-51f3-4714-9a35-6615075bf93e

Public Version Date

February 07, 2019

Public Version Number

2

DI Record Publish Date

March 26, 2018

Package DI Number

26939029817482

Quantity per Package

2

Contains DI Package

16939029817485

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton