Catalog Number

-

Brand Name

Well at Walgreens

Version/Model Number

786610

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

LDE

Product Code Name

Stethoscope, Manual

Public Device Record Key

b9e18d3a-556c-41f6-8e95-19332a4b328e

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

May 15, 2020

Package DI Number

10311917206179

Quantity per Package

24

Contains DI Package

00311917206172

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Carton