Catalog Number

-

Brand Name

Eufy

Version/Model Number

T9140

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

MNW

Product Code Name

Analyzer, Body Composition

Public Device Record Key

3ce94e04-00df-49c7-a1e6-f99689e16161

Public Version Date

March 27, 2020

Public Version Number

1

DI Record Publish Date

March 19, 2020

Package DI Number

16947468554793

Quantity per Package

1

Contains DI Package

06947468554796

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

1pcs/box