Catalog Number

74-037

Brand Name

Meijer

Version/Model Number

74-037

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

NUH

Product Code Name

Stimulator, Nerve, Transcutaneous, Over-The-Counter

Public Device Record Key

c68b0bd1-c2d3-4beb-8489-fa930ec06cb0

Public Version Date

February 19, 2021

Public Version Number

3

DI Record Publish Date

September 15, 2016

Package DI Number

30708820944788

Quantity per Package

4

Contains DI Package

00708820944787

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Intermediate