Catalog Number

SEN 2002

Brand Name

TetraSens

Version/Model Number

TetraSens

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

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

K190795,K190795

Product Code

KOI

Product Code Name

Stimulator, Nerve, Peripheral, Electric

Public Device Record Key

9efb9cdb-7124-4fa4-8993-61ef30caa484

Public Version Date

October 02, 2020

Public Version Number

2

DI Record Publish Date

April 23, 2020

Package DI Number

07350012440039

Quantity per Package

20

Contains DI Package

07350012440022

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box