Catalog Number

A230.66

Brand Name

V. Mueller

Version/Model Number

A230.66

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 18, 2019

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

-

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

BWA

Product Code Name

UNIT, ELECTROSURGICAL ANDCOAGULATION, WITH ACCESSORIES

Public Device Record Key

954b096b-0fbb-4c38-84e0-b8054031a62a

Public Version Date

March 24, 2020

Public Version Number

3

DI Record Publish Date

October 11, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-