Catalog Number

610BKHOP

Brand Name

Essentials

Version/Model Number

610BKHOP

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

aefc0e9e-bdb6-469d-aa5c-4d153cd9ad35

Public Version Date

September 07, 2020

Public Version Number

1

DI Record Publish Date

August 29, 2020

Package DI Number

00634782599607

Quantity per Package

20

Contains DI Package

00634782098223

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case