Catalog Number

9187-CME

Brand Name

SPRINT™

Version/Model Number

Test Cable

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"

Yes

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

-

Product Code

NHI

Product Code Name

Stimulator, Nerve, Electrial, Percutaneous (Pens), For Pain Relief

Public Device Record Key

44e5fa67-b824-4b47-a8fc-73bf7e596ae2

Public Version Date

January 08, 2021

Public Version Number

7

DI Record Publish Date

January 19, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-