Catalog Number

-

Brand Name

StimRouter

Version/Model Number

ST2-SW01

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

GZF

Product Code Name

STIMULATOR, PERIPHERAL NERVE, IMPLANTED (PAIN RELIEF)

Public Device Record Key

d3ec6f75-51b7-4a78-a4be-85dc8164654a

Public Version Date

September 20, 2021

Public Version Number

4

DI Record Publish Date

February 08, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-