Catalog Number

-

Brand Name

Virtuosaph Plus with Radial Indication

Version/Model Number

VSP550EX

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

K160206,K160206

Product Code

GEI

Product Code Name

Electrosurgical, Cutting & Coagulation & Accessories

Public Device Record Key

1920153d-4c71-44d3-ac91-fe31566f0c26

Public Version Date

February 07, 2019

Public Version Number

5

DI Record Publish Date

October 12, 2016

Package DI Number

50699753450764

Quantity per Package

5

Contains DI Package

00699753450769

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

5 Piece Case