Catalog Number

-

Brand Name

Braun

Version/Model Number

BNT100US

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

FLL

Product Code Name

Thermometer, Electronic, Clinical

Public Device Record Key

e2ecd17b-ac4c-4276-936b-4de0c7ffd760

Public Version Date

February 10, 2021

Public Version Number

1

DI Record Publish Date

February 02, 2021

Package DI Number

10328785006657

Quantity per Package

6

Contains DI Package

00328785006650

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case