Catalog Number

-

Brand Name

Well at Walgreens

Version/Model Number

MDPS100

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

Yes

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

GXY

Product Code Name

Electrode, Cutaneous

Public Device Record Key

59cd234d-275f-4d25-a9ec-9ae397ec895f

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

August 16, 2016

Package DI Number

10311917178681

Quantity per Package

48

Contains DI Package

00311917178684

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case