Catalog Number

-

Brand Name

PremierPro

Version/Model Number

6802

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"

Yes

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

04478d3a-6427-4689-a9bd-815ac6453991

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

June 15, 2016

Package DI Number

10818566013337

Quantity per Package

500

Contains DI Package

00818566013330

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case