Catalog Number

-

Brand Name

Greater Goods

Version/Model Number

0615

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)

-

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

a1e94add-500f-4eb1-8eae-fea72fa3ad1f

Public Version Date

November 10, 2020

Public Version Number

1

DI Record Publish Date

November 02, 2020

Package DI Number

10875011006153

Quantity per Package

24

Contains DI Package

00875011006156

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-