Catalog Number

-

Brand Name

Vercise Genus™

Version/Model Number

DB-1408

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

P150031,P150031

Product Code

MHY

Product Code Name

Stimulator, electrical, implanted, for parkinsonian tremor

Public Device Record Key

71e3ba69-4a32-4ac3-aef8-26a3ed6a9032

Public Version Date

October 29, 2021

Public Version Number

2

DI Record Publish Date

January 28, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-